Registered for transniissian by post as a magazine. TRANSACTIONS AND PROCEEDINGS OF THE NEW ZEALAND INSTITUTE VOL. LI (New Issue) EDITED ANP PUBLISHED UNDER THE AUTHORITY OF THE BOARD OF GOVERNORS OF THE INSTITUTE ISSUED 1st SEPTEMBER, 1919 latUington, ^.%. MARCUS F. MARKS. GOVERNMENT PRINTING OFFICE William Weslet and Son, 28 Essex Street, Strand, London W.C. MEMORANDUM FOK AUTHORS OF PAPERS. 1. All papers must be typewritten, unless special permission to send in written papers lias been granted by the Editor for the time being. 2. The author sliould read over and correct the copy before sending to the Editor of the Transactions. 3. A badly arranged or carelessly coaiposed paper will be sent back to the author for amendment. It is not the duty of an editor to amend either bad arrangement or defective composition. 4. In regard to underlining of words, it is advisable, as a rule, to underline only specific and generic names, titles of books and periodicals, and foreign words. 5. In regard to specific names, the International Rules of Zoological Nomenclature and the International Rules foi- Botanical Nomenclature must be adhered to. 6. Titles of papers should give a clear indication of the scope of the paper, and such indefinite titles as, c.y., " Additions to tbe New Zealand Fauna " should be avoided. 7. Papers should be as concise as possible. 8. Photographs intended for reproduction should be the best pro- curable prints, unmounted and sent flat. 9. Line Drmvings. — Drawings and diagrams may be executed in line or wash. If drawn in line — i.e., with pen and ink — the best results are to be obtained oidy from good, firm, black lines, using such an ink as Higgin's liquid India ink, or a freshly mixed Chinese ink of good quality, drawn on a smooth surface, such as Bristol board. Thin, scratchy, or faint lines must be avoided. Bold work, drawn to about twice the size (linear) of the plate, will give the best results. Tints or washes may not be used on line drawings, the object being to get the greatest contrast from a densely black line drawn on a smooth, white surface. 10. Wo,sh Draiviugs. — If drawing in wash is preferred, the washes should be made in such water-colour as lamp-black, ivory black, or India ink. These reproduce better than neutral tint, which inclines too much to blue in its light tones. High lights are better left free from colour, although they may be stopped out with Chinese white. As in line drawings, a tine surface should be used (tlie grain of most drawing- papers reproduces m the print with bad effect), and well-modelled contrasted work will give satisfactory results. 11. Size of Draioings. — The printed plate will not exceed 7^ in. by 4-| in., and drawings for plates may be to this size, or preferably a multiple thereof, maintaining the same proportion of height to width of plate. When a number of drawings are to appear on one plate they should be neatly arranged, and if numbered or lettered in soft pencil the printer will mark them permanently before reproduction. In plates of wash iv Memorandum for Authors of Papers. drawings, all the subjects comprising one plate should be grouped on the same sheet of paper or cardboard, as any joiuing-up shows in the print. Text figures should be drawn for reduction to a width not exceeding 4^ in. If there are a number of small text figures they should be drawn all for the same reduction, so that they may be arranged in groups. 12. Majis. — A small outline map of New Zealand is obtainable at a low price from the Lands and Survey Department, Wellington, upon which details of distribution, &c., can be filled in according to the instructions given above for line drawings. 13. Citation. — References may be placed in a list at the end of an article or arranged as footnotes. The former method is preferable in long papers. In the list references are best arranged alphabetically, reference in the text being made by writing after the author's name, as it occurs, the year of publication of the work, adding, if necessary, a page number, and enclosing these in parentheses, thus : " Benham (1915, p. 176)." Example of forms of citation for alphabetical list : — Benham, W. B., 1915. Oligochaeta from the Kermadec Islands, Trans. N.Z, Inst., vol. 47, pp. 174-85. Park, J., 1910. The Geology of New Zealand, Christchurch, Whitcombe and Tombs. When references are not in alphabetical order the initials of the author should precede the surname, and the year of publication should be placed at the end. 14. In accordance with a resolution of the Board of Governors, authors are warned that previous publication of a paper may militate against its acceptance for the Transactions. 15. In ordinary cases twenty-five copies of each paper are supplied gratis to the author, and in cases approved of by the Publication Com- mittee fifty copies may be supplied without charge. Additional copies may be obtained at cost price. T K A N 8 A C T I () N S AND PROCEEDINGS OF THE NEW ZEALAND INSTITUTE VOL. LI (New Issue) EDITED AND PUBLISHED UNDER THE AUTHORITY OF THE BOARD OF GOVERNORS OF THE INSTITUTE ISSUED 1ST SEPTEMBER, 1919 Wellington, f.l. MARCUS F. MABK8, GOVERNMENT PRINTING OFFICE William Wesley and Son, -28 Msskx Street, Strand, London W.C. ALEXANDER HORSBURGH TURNBULL. \Fnce p. rii. OBITUARY. ALEXANDER HORSBURGH TURNBULL. 1868-1918. Alexander Horsburgh Turxbull was born in Wellington on thr I Ith September. I8(i8. and was educated at Duhvicli ("olleae, England. HivS father was Mr. Walter Turnbull. one of the founders of the linn W. and G. Turnbull and Co. (now Wright. Stephenson, and Co.) : and on his entering on a nicrcantile career Mr. Turnbull joined his fathers London offic<', returning to Wellington in 1890. For luanv vears he was associated with the late Mr. Nicholas Reid in the nianagenient of the business of W. and (i. Turnbull and Co., but owing to failing health he was compelled some eighteen months before his death to relinquish most ot his business activities retiring altogether in October. 1917. The whole of his activities and the considerable means i-esulting from his business were then devoted to the augmenting of his collection of books of history, travel, and literature. He became one of the best-known book-collectors of New Zealand, and his library was known far beyond the limits of New Zealand. He devoted himself largely to the gathering of a representative collection of accounts of voyages to the islands of the Pacific, and the histories of those islands, including .Vustralia and New Zealand : and thi' collection gathered by him is reputed to be one of the best in the world. Jt includes not only works in English, but many in Dutch, French, .Spanish. German, and other languages, the Dutch being especially valuable. This portion forms, however, only about one-fourth of the library, the rest being devoted to histories of early colonization in various countries, and to poetry and general literature. Besides having copies of every obtain- able edition of the better-known poets, the library is rich in works of the minor poets. His collection of autographs, letters, ])oems, logs, and journals is most representative : and he secured many rare editions l)oth of well- known and out-of-the-way writers, so that the library contains wealth for the historian and for the lover of [)ure literature as well as for the bibliophile. He also specialized in New Zealand and Australian paniphlets, original drawings, and sketches of early New Zealand and Australia, maps, charts, photographs, &c. The library contains over 32,000 bound volumes, thousands being almost jewel-like in their artistic binding, the work of such well-known firms as Zaehnsdorf and Riviere, of London : thousands of unbound |*amphlets, leaflets, maps, etchings, drawings, and prints, all of inestimable value from an historical point of view. Whilst Mr. Turnbull was a member of the Wellington Philosophical Society from 1897 to the dav of his death, he was not an active member so far as the reading of papers was concerned. He was, however, inde- fatigable in the gathering together of this s])lendid collection, which he com- menced whilst still in London, and the luunber and extent of manuscript notes in the various volumes show that he was a wide and unremitting reader who loved his books and knew them thoroughly. Apparently his sole object in making the collection, apart from present pleasure, was the viii Ohituart/. eventual presentation of it to the Dominion. Not only did he at all times place the library at the disposal of students and researchers, but by his knowledge of the contents of the books lie was able to render them valuable assistance, and never refused to do so. Whilst, therefore, he did no original creative work, he did what was even more important — gathered a wealth of material that will give inspiration for original work for many vears to come. This wealth he bequeathed to His Majesty the King in trust as a reference library to be housed in Wellington. The bequest is the most valuable by which the city of Wellington has ever benefited, and one of the most valuable ever made in the Dominion. Mr. TurnbuU possessed an extensive collection of Maori carvings, weapons, im])lements, articles of clothing, and other objects of ethnological value, and this collection he presented to the Dominion Museum in January, 1913. His desire for anonymity was respected, but it is due to his memory that this shoidd now be known. He was also a prominent member of the New Zealand Academy of Fine Arts, and had gathered a valuable collection of pictures by New Zealand and other artists. Many of these pictures, which deal with matters of historic interest to New Zealand and Australia, passed with his bequest and are now housed in the library which is known after the donor as the Turnbull liibrary Mr. Turnbull died in Wellington on the 28th June, 1918. He was a Fellow of the Linnean Society and a Fellow of the Royal Geographical Society ; and, whilst his name does not appear among the illustrious in the world of science, the original work that will result from his labours and pleasures of collecting will certainly enrich the world of science no less than its sister world of literature. Johannes C. Andersen. Obituary. , ■ i^ HENRY SUTER, 1841 1918. Wriii the issue (il tlic 1 wcuty-sccoiid x-oliiinc (if the Transactions a new star ruse on the coiu'liological world. I''(ii' licic. undei- a \v,\nw liithcrto unknown, appeared a series of excellent dcsciiptions of small land-shells, illustrated with unusually clear and detailed drawinjrs by the same hand. In continu- ation an account followed of the jaws and radula of various miiiute snails. This very difficult work was beautifully done. These contributions, signed " H. Huter,'" wen^ waiiiily welcomed by a little band of zoological research workers in Australasia. in answer to iiujuivies as to who our new cojurade was. Captain Hutton replied that he was a 8wiss. lately arrived in New Zealand with introductions from well-known European zoologists. Henry Buter was born on the 9th March, 1841, and. was the son of a prosperous silk-manufacturer of Zurich. He was educated at the local school and universit\'. being trained as an anah'tical chemist. He joined the business of his father, and for some years engaged in various commercial pursuits. From his boyliood he was deeply interested in natural historw He enjoyed the friendshi]) and helj) of such men as Dr. August Forel, Professor Paul Clodet, the brothers de Saussure, Escher von der Linth, and eapeciall}' the well-know'n conchologist Dr. Albert Mousson. Partly to improve his financial [)ros]5ects and jjartly lured by the attraction of the fauna of a new country. 8utei' resolved to emigrate to New Zealand. It was the last day of the year 1886 when with his wife and a family of young children he landed in New Zealand. He began his colonial career by taking u}) a remote selection in the Forty-mile Bush, in the Wairara])a district. It is only in a story that a middle-aged townsman can ever turn backwoodsman with success, and so aftei' about a year Suter relinquished the hard and hopeless struggle. At this critical time Captain Hutton, always a firm friend to zoologists, succeeded in obtaining for his protege a ])ost as assistant manager at the Mount Cook Hermitage. Subsequently work was available at the ( 'anter- bury Museum. After that, at one or another of the scientific institutions of New Zealand Suter spent the remainder of his life at congenial employ- ment. Henry Suter was an expert collector. He excelled in taking the minutest land-shells, to find which requires knowledge, patience, and the sharpest eyes. Specialists in other groups were often supplied hy Suter with valuable material. In Switzerland he had formed a fine collection of European land and fresh- water shells. This was afterv,'ards acquired by the Australian Museum. For several years Suter restricted his studies to the terrestrial and Huviatile Mollusca of his adopted country. When his work on these approached completion he proposed to extend his investigations to land Mollusca abroad. Hence his scattered papers on land Mollusca from Brazil, South Africa, and Tasmania. His friends, however, persuaded him that science would be better served if he relinquished the foreign shells and transferred his attention to the marine Mollusca of New Zealand. Not only did he take this course, but he finally embraced the Tertiary Mollusca also in his sphere of operations. Inset i — Tran.s. X Obituary. Glancing over his ))aper,s, it is apparent that his writings were largely modelled on those of his distinguished predecessor. Captain Hutton. It was indeed fortunate that the work of the one should have succeeded that of the other without the intervention of what the geologists describe as an unconformity. Perhaps at no time did Suter quite realize the undiscovered residue of the fauna on which he worked. In his various reviews and revisions and supplements he wrote as if he had in hand if not all at least almost all the species of the area under examination. Patience, perseverance, and concentration, rather than any great breadth of view, were his characteristics. His magnum opus, the Manual of ihe Nev^ Zealand MoUnsca* was approached by a whole quarter-century of study and labour. It was the late Mr. .Vugustus Hamilton who planned the Manual, and obtained from the Government the means for its production. A com])etent critic wrotef of this magnificent volume that it made an extraordinary advance in Antipodean conchology. The nomenclature of the subject was raised to a modern standard, so that by its guidance any one can now correctly name the shells of New Zealand. Suter needs no other eulogy than his Manual. After the Manual was completed he was engaged l)y the Geological Survev to describe collections of Tertiary Mollusca gathered by the Department. Gn this he was busy for the remainder of his life, and the results are embodied in three Palaeonfological Bulletins of the Geological Survey. After a l)rief illness Henry Suter passed away at his home in Christ- church on the 30th July, 1918. Charles Hedley. ♦Published in 1913-15. '\Journ. of Conch., vol. 14. p. 287. 1915. HENRY SUTER. Fuce p. x. THOMAS WILLIAM ADAMS. Obituary. xi THOMAS WILLIAM ADAMS, 1841-1919. Thomas William Adams was born in 1841 at Grravely, Cambridgeshire, England. He was educated first at a private school in Cambridge, and later at the British and Foreign Normal School. London. In 1862 he arrived at Lvtteiton, and soon aftei' took up land at Gi'eendale, on the Canterbury Plain, where he successfully followed farming for many years. The necessity for jn-oviding shelter for his stock against the frequent high winds showed Mr. Adams, as it did many of tlie ])ioneers, that the planting of shelter-belts was essential. A little later tree- planting was encouraged by the Government of the day by means of land grants in proportion to th<' area phuited. As time went on he was not content to ])lant oidv the usual trees, but, stimulated l)y the true spirit of research, he Sought to hnd out wh.at other trees were suited to the conditions sup- plied by his neighbourhood — an area typical of much of the Canterbury Plain. So it came about that before many years had passed by he had growing upon his property pretty well all the exotic trees which at that time had been introduced into New Zealand. This made it necessary for him to go fartlier afield for his material, and he got into touch with some of the most celebrated arboriculturists of the day, and also botanical collectors in little-known regions, so that seeds of many species of trees and shrubs came yearly into his hands. As the years passed by, tlumks to his love for the self-imposed task and to his superabundant energy, his Greendale estate not only possessed fine mixed plantations, but easily the largest collection of living specimens of exotic trees and shrubs in New Zealand, representing not unworthily the hardy tree and shrub flora of the world. In conjunction with this practical work Mr. Adams became a close student of the literature relating to that class of plants which interested him so greatly, so that no one in the Dominion possessed sucli a wide knoAvledge of the subject. Nor did he neglect the broader aspects of his ])ursuit. Here his researches with regard to the Monterey j)ine {Pirins rddiafa) as a timber-tree can without hesitation be declared the most important advance which forestry has made in New Zealand u]) to the present time, and one which will eventually add great wealth to the country. That a tree universally despised as economically worthless (unless for inferior firewood) should, through Mr. Adams's experiments and unceasing advocacy of its value, come to be recognized by all New Zealand foresters as a most important timber-tree speaks volumes as to his acumen and careful investigations. Indeed, Mr. Adams through his teaching regarding the value of the Monterey pine materially modified the forestry policy of the Dominion. Here was a tree, hardly used in the early forestry operations, whose rapidity of growth combined with the many uses of its timber made its planting on the largest scale a highly payable proposition easy of demonstration. In 1897 Mr. Adams joined the Canterbury branch of the New Zealand Institute. Though living too far from Christchurch to take an active part in the management of the Philosophical Institute of Canterbury, he attended the meetings whenever possible, read papers at times, delivered addresses, and showed interesting exhibits from his arboretum. Several of his papers appear in our Transactions, one in the Report of the Australasian Association for 1904, and a number in the Journal of the Canterbunj Agricultural and Pastoral Association. These papers form a xii Ohitiiary. record of most important work, and give valuable details regarding the growth and behaviour of many species of economic trees. Apart from their economic value they have also a considerable phytogeographical bearing. On account ol his valuable work in arboiicuitiiiv Mr. Adaiu,s sonic Nciiis ago was elected an honorary member of the Hoxal Diitish Arboricultural Society, and last year he was made a life meml)er of tlie New Zealand Forestry League. As a public man Mr. Adams took great interest in education. He was for twenty -six years a member of the North Canterliurv Education Board, and for twenty years a member of the Board of Governors of Canter burv College. To this institution he left by will 100 acres of land at Greendale on which are many of his plantations, and his entire general collection of trees and shiubs. To this bequest was added the sum of £2,000. the mone\- and the land with its collections to form the nucleus of a forestr\- scliool in connection with Canterbury College. In 1913 he was one of the members of the Royal Commission on Forestry, and was of the greatest service to the Commission both from his knowledge and clear judgment. Mr. Adams, who liad been far from well for some time, passed away on the 1st June, 1919. His end was not altogether unexpected by his friends, notwithstanding he had attended the Science Congress in February, and gone to Dyer's Pass on one of the excursions. His lamented death has left a gaj) in New Zealand science which will not readily l)e filled. No man was more resj.'ected ; few of our members have rendered more disinterested service to their countr^•. L. COCKAYXK. CONTENTS, ANTHROPOLOGY. PAGES Art. XXVI. The Edible Fish, &c.. of Taupn-mii-a-Tia. By H. J. Fletcher . . 259-264 XXVIII. Some Maori Fish-hooks from Ota.iro. By H. D. Skinner .. 267-268 XXX^'I. Some Notes on thelLanoiiajic (jf the ( 'hatliam Islands. By H. W. Williams . . . . . . . . " . . 415-422 BOTANY. Art. IX. Contributions to a Fuller Knowledge of the Flora of New Zealand: No. 6. By T. F. flheeseman, F.L.S., F.Z.S. .. 85-92 X. Some Additions to the New Zealand Flora. Bv T. F. Cheese- man. F.L.S.. F.Z.S. .. .. .. ■ .. .. 92-95 XI. A New Variety of Ptens iiiucilriitti. By H. Carse . . . . 95 XIV. Descriptions of New Native Flowering-plants. By D- Fetrie, M.A.. Ph.D. .. .. .. ■ .. .. 106-107 XVIII. Notes on the Autecology of certain Plants of the Peridotite Belt. Nelson : Part I — Structure of some of the Plants (No. 2). By M. Winifred Betts. M.Sc. . . . . 136-156 XX. Studies in the New Zealand Species of the Genus Li/ropodi/iim : Part III— The Plasticity of the Species. By the Rev. J. E. Holloway, D.Sc. . ." . . . . " . . . . 161-216 XXXIV. The Vegetation of Banks Peninsula, with a List of Species (Flowering-plants and Ferns). By R. M. Laing, B.Sc. . . 355-408 XXXV. The Pronunciation of Scientific Terms in New Zealand, with Special Reference to the Terms of Botany. By A. Wall . . 409-414 XXXVIII. A History of Hagley Park, Christchurch, with Special Refer- ence "to its Botany. By Miss E. M. Herriott, M.A. . . 427-447 GEOLOGY. Akt. II. The Significant Features of Reef-bordered Coasts. By W. M. Davis . . . . . . . . . ." . . 6-30 V. On the Occurrence of Thin Bands of Marble at South Peak, near Hampden. Otago. By J. Park. F.G.S. . . . . . . 41-42 VII. Description of a 'New Species of the 'Family Cerithiidae. By H. Suter '. . .. ..".'. . . .". 68 XII. New Fossil Mollusca. By J. A. Bartium . . . . . . 96-100 XIH. A Fossiliferous Bed at Kawa Creek. West Coast, South of Wai- kato River. New Zealand. By J. A. Bartrum . . . . 101-106 XV. Further Notes on the Horowhenua Coastal Plain and the Asso- ciated Physiographic Features. By C. L. Adkin .. .. 108-118 XIX. Further Notes on the Geology of the Trelissick or Castle Hill Basin. By R. Speight, M.Sc. .. .. .. .. 1.57-160 32413 XIV Contents. AiiT. A'XUI. Fauna nf the Hampden Beds and Classification of the Oamaru pages System. By P. Marshall, M.A., D.Sc, F.G.vS. . . . . 226-250 X.\[\'. OcciiiTcnce of Fossil Moa-bones in the Lower Wanganui Strata. My W Marshall. M.A., D.Sc, F.G.S. . . . . . . 250-253 XW. Some New Fossil Species of Mollusca. Bv P. Marshall, M.A., D.Sc, F.G.S., and R. Murdoch . . " . . . . . . 253-258 XXiX. The Older Gravels of North Canterbury. By R. Speight, M.Sc, F.G.S. .. .. .. .. .. .. 269-281 .\X.\. Hough i^idge, Otago, and its Splintered Fault-scarp. By C. A. Cotton .. .. .. .. .. " .. 282-285 X.X.XI. Note nil the Mechanical Comjwsition of the so-called Loess at Tiniaru. By L. J. Wild, M.A., B.Sc, F.G.S. . . . . 286-288 XXXII. The Geology of the Middle Clarence and Ure Valleys, East Marlborough, New Zealand. Bv J. Allan Thomson, M.A., D.Sc, F.G.S. . . . . .". . . . . . . 289-349 XX.WTI. Report nn the Natural Features of the Arthur's Pass Tunnel. Bv C. C. Farr, F. (J. Hogg. S. Page, L. J. Wild, and F. W. Hilgendorf . . . . . . . . . . . . 422-426 XL. Terminology for lieak and J'"oraminal Dev'clopment in Brachio- poda. ■ By S. S. Bnckman, F.G.S. . . . . . . 450-454 ZOOLOGY. Art. II J. On tiic Occurrence oi Two Unusual Blood-vessels in Hyla aurea. By W. B. Benham, D.Sc, F.R.S. . . . . . . 30-34 I\'. Some Earthworms from Stejihen Lsland and D'Urville Island. By W. B. Benham. D.Sc, F.R.S. . . . . . . 35-41 ^'T. A l*reliminar\ Investigation of the Age and Manner of Growth of Brown Trout in Canterburj', as shown by a Microscopic E.xaminatioii of their Scales. By M. H. GodV- M.A., B.Sc. 42-67 \'III. The Structuie of Am jihllmhi rrpjiata Martvn. Bv Winifred C. Farnie. M.A. . . . . . . ■..".. . . 60-85 X\l. Cfhid. an Abeirant Genus of the Amphipodan Family Talitridae. By C. Chilton. M.A.. D.Sc, LL.D., F.L.S. . . . . 118-129 X\'ll. New S])ecies of Mollusca, from various Dredgings taken off the Coast of New Zealand, the Snares Islands, and the Bounty Islands. By Miss M. K. Mestayer .. .. .. 130-135 XXI. Notes on the Birds of South-western Otago. By A. Philpott .. 216-224 XXII. Descrii)tion of New Species of Lepidoptera. By A. Philpott . . 224-225 XXXIII. Descriptions of New Zealand Lepidoptera. By E. Meyrick, B.A., F.R.S. .. .. .. .. •■ ■■ 349-359 XX.XIX. A New Discoglossoid Fron from Xcw Zealand. By A. R. McCullocli . . . . . . . . . ." . . 447^49 MISCELLANEOUS. Airr. I. On tlic Toxicity of the Tutu Fruit and Seed. By J. Malcolm, M.D. 1-5 XX\II. To wtiat extent is Earth-rotation the Cause of the Ocean Cur- rents? Bv A. W. Burrell .. .. .. •- 264-267 Contents. x\ PROCEEDINGS. Sixteenth Annual Meeting of the Board of Governors Proceedings of the New Zealand Institute Science Congress Annual Address of the President Wellington Philosophical Society Auckland Institute Philosophical Institute of Canterbury Otago Institute Hawke's Bay Philosophical Institute Manawatu Philosophical Society Wanganui Philosophical Society Nelson Institute l!H!) I'Al 4r)7 472 478^85 48;"}^ 95 49(» 49H 499 -502 503 -504 505 500 50t> 507 508 508 APPENDIX. New Zealand Institute Act and Regulations Hutton Memorial Medal and Research Fund Hector Memorial Research Fund Regulations for administering the Government Research Grant Carter Bequest New Zealand Institute — List of ( )fificers, &c. Roll of Members Serial Publications received by the Library of the Institute List of Institutions to which the Publications of the Institute are present ci I Index 511 ill 513 jl.i 515 115 5l(j 5I() J17 520 521- 535 >36-539 >40- .545 -i47- 548^ LIST OF PLATES Alexander Horsburgh Turnbbull . . Hexrv Suter Thomas Wflliam Adams M. H. (JUDBY — Plate I— Fig. 1. Brown trout, Selwyn River Fig. 2. '■ Disf)lacement "" scale, Rakaia River I'late 11— Fig. 1. Brown trout. Selwyn River Fig. 2. Bro\vn trout, Selwjoi River Plate III— Fig. 1. Brown trout, Selwyn River Fig. 2. Brown trout, Lake EUesraere Plate IV— Fig. I. BrowTi trout, Opihi River . . Fig. 2. Brown trout, Rakaia River Plate V— Fig. 1. Brown trout, Mary mere Fig. 2. Brown trout, Marymere Plate VI— Fig. 1. Brown trout. Lake Coleridge Fig. 2. Brown trout. Lake Coleridge J. Bartrtji — Plate \' 11. — New fossil Mollusca M. K. Mestayer — Plate VIll. — New species of Mollusca . . J. E. HoLl.nWAY — Plate IX— Fig. 1. Lycopodiuni carium and L. varium var. polaris Fig. 2. L. Selago and L. ? varium . . Plate X— Fig. 1. Lycopodium Selago Fig. 2. L. Billardieri. L. Billardieri vai\ gracile, and L. Phleginaria Plate XI. — Lycopodium, cernuum Plate XII— Fig. 1. Lycopodiu))!, laterale and L. raniulosuin Fig. 2. L. volubile and L. scariosum Plate XIII. — Lycopodiu»n densum Plate XI\^ — Lycopodium fastigiahim and L. Drum,mondii P. Marshall — Plate XV. — Fossils from the Hampden beds Plate XVI. — Fossils from the Hampden beds Plate XVII. — Fossils from the Hampden beds Plate XVIII. — Part of femur of moa from lower Wanganui strata . . FOLLOWS PAfiE vi X X 48 48 48 48 48 48 48 48 54 54 54 54 100 134 168 168 168 168 180 180 180 192 192 234 234 234 -Will List of Plates. I'. -Marshall and H. .Mckdoch — I'late XIX. — New fossil species of Mollusca Plate XX. — New fossil species of Mollusca Plate XXI. — New fossil species of Mollusca A. \V. Blirrell — Plate XXII. — Working model showing ocean currents H. 1). Skinner — Plate XXIII. — .Maori Hsh-hooks from Otago .1. A. Thomson — Plate XXIV— Fig. I. The suniinit of Mount Tapuaenuku . . Fig. 2. Cliff i)f '" syenite," Mount Tapuaenuku Ji'late XXV— Fig. 1. View of Coverham, looking westward Fig. 2. Junction between Clarentian and pre-Notocene Plate XXVI— Fig. 1. Chalk Range, from the south-south-east Fig. 2. Ff)lding in the Sawpit Gully mudstones Plate XXVIl. Cliffs on left bank of Isolated Hill Creek Plate XXVIII.— Isolated Hill from Isolated Hill Creek . . Plate XXIX— Fig. 1. The ritlgc between the Dee and the Liniburne Fig. 2. Great Mailborough conglomerate in the Dee Gorge A. H. McCULLOCH— Plate XXX. — LiujifhiKi IiamiUoni n. sp. FOLLOWS PAGE . 258 . 258 . 258 266 268 308 308 308 308 316 316 316 326 326 326 448 TKANS ACT IONS. Tl^AlSl SACTIONS OF THE NEW ZEALAND INSTITUTE Art. I. — On the Toxicity of Tutu Fruit and Seed.^ By Professor John Malcolm, M.D., Physiology Department, University of Otago. [Read before the Otago Institute, 10th September, 1918; received by Editors, 13th September, 1918 ; issued separately, 14th Ulay, 1919.] Attention has frequently been drawn to the remarkable fact, discovered by the Maoris, that the juice of the ripe tutu-berry is harmless, while the seed is intensely toxic. It says much for the intelligence and powers of observation of that race that such a discovery should have been made. Perhaps the pos- session of subjects of experiment in the form of prisoners of war played a part in establishing the fact. As the writer had already reported some experiments on the toxicity of shoots a,nd leaves of Coriaria ruscifoUa and C. angustissima, the opportunity was taken last summer of collect- ing some of the fruit in order to test the degree of toxicity of the seed of C. ruscifoUa, and at the same time to examine the juice. The material was obtained by stripping the so-called " berries " off the stalks of the racemes (sample I), and in another case (sample II) by simply shaking twigs laden with fruit inside the calico collecting-bag. In the latter case only the fully ripe berries dropped off. The juice was expressed by simple pressure on the bag, and the seed vvas obtained from the remainder by washing and kneading the bag till the strainings were almost colourless. By suspension in water it was then comparatively easy to separate the seed from other debris, for the latter renjained suspended for a longer time than the seed. A consider- able proportion of the seeds rose at once to the top and floated there, but the bulk of them sank rapidly to the bottom. The seed was dried in the air, and thus preserved for future use. The Juice. A known quantity of the juice as first expressed from the bag was evaporated down on a slow fire. The reaction remained acid during the * The expenses incurred in this research were defrayed out of a Government grant made through the New Zealand Institute. 1— Trans. 2 Transactions. evaporation. It did not seem to form a jelly at any stage in the evapora- tion, and merely thickened to a stiff syrup. In this state it did not grow moulds, although weaker concentrations readily did so and also readily underwent fermentation with brewers' yeast. After standing some weeks the syrup became crystalline, but the crystals were mingled with so much precipitated material and pigment, and recrystallization was so slow, that it was difficult to obtain a quantity of the purified crystalline substance. The small quantity that was obtained evidently consisted of glucose, as shown by its physical appear- ance and its osazone crystals. That laevulose was also present in the crude syrup was, however, clearly shown by the following observation : The syrup was extracted with hot alcohol, clarified with charcoal, and examined in the polarimeter in watery solution ; the result was laevo- rotation ; and the solution gave very distinctly Seliwanoff's test for laevulose. That this solution contained a mixture of dextro- and laevo- rotatory sugars was proved by the fact that in a clear solution contain- ing 15-5 per cent, reducing-sugar as estmiated by Allihn's method the rotation corresponded to only 2-3 per cent, laevulose. The syrup was also tested for galactose by the mucic-acid test, but with negative results, so that no evidence was found of the presence of raftinose. The ash of the juice was found to contain a considerable amount of iron salts. Two experiments were made in order to test whether the concentrated juice contained any of the poisonous properties of the other parts of the plant. In one a known amount of the crude syrup was diluted and administered by stomach-tube to a rabbit. No symptoms followed. The dose corresponded to about 54 grammes of the juice as expressed from the ripe fruit. It would correspond to about 2 lb. to a human adult. In the other an attempt was made to extract any tutin that might be present. The quantity used would correspond to about 1 kilogram (2-2 lb.) of the original juice. It was covered with acetone in a stoppered bottle, and left for three weeks, with frequent stirring and shaking. The extract so obtained was heated to drive off the acetone, dissolved in water, and administered to a rabbit. No symptoms resulted which could be ascribed to tutin. The animal became practically anaesthetized and unconscious, but recovered fully in a few hours. The symptoms were probably due to some acetone or acetone compounds which had not been completely removed by the heating. From these experiments it seems extremely unlikely that the juice contains any tutin. Toxicity of the Seed. After trying the hypodermic injection of solutions obtained by various methods of extracting the tutin, the conclusion was arrived at that oral administration of the seed would be the best in this case, as it resembled more closely the natural way in which poisoning might occur. Accord- ingly, since rabbits could not be induced to swallow the amount of seed required, a watery extract containing suspended matter was made by grinding the dose of seed in a coffee-mill, adding successive small quan- tities of water, and straining the extracts through cheesecloth. In this way the pulverizable part of the seed was separated from the husk, and a muddy-looking suspension was obtained which could be administered to the rabbit by stomach-tube. The residue left on the straining-cloth was considerable ; in several cases where it was collected and dried it Malcolm. — Toxicity of Tutu Fruit and Seed. 3 amounted to 50 to 60 per cent, of the whole dose of crushed seed. In order to test whether such residues contained any appreciable amount of tutin, a fairly large amount was dried, extracted with ether, and the ether-soluble material administered to a rabbit in watery suspension by stomach-tube. It produced no symptoms whatever in a dose equal to 7'5grm. of "husk" per kilogram body weight, so that the bulk of the tutin may be supposed to have been present in the watery suspension. When the seed was administered in this way the results shown in the table were obtained. Toxicity op Seed. No. Blaterial used. Dose per Kilogram, iu Grammes. 1 Result. Estimated Per- centage of Tutin in Seed. 256c Sample I 3-7 Death in three hours . . 016 267 270 •295 Sample II 3-7 4'0 4-3 Slight, if any, symptoms Distinct minor symptoms Death in about three hours o'l4 0-16 272 4-5 Symptoms more marked than in 0-12 274 282 " 50 6-5 exp. 270 Severe symptoms, but recovered Death in three hours . . Oil 0-10 296 Green seed 6-0 Death in one hour and a half . . 0-125 * This animal had been used for exp. 274, and had then had its thyroid gland removed, about four weeks before being used for exp. 29.5. The percentages of tutin in these experiments have been calculated from the results of previous work by Fitchett and other experiments by the writer. The standards adopted for rabbits wei-e that a dose of 6 milligrams per kilogram produces no marked symptoms ; 6 milligrams produces symptoms in one hour and a half, and is ultimately fatal ; 7'5 milligrams produces symptoms in about half an hour, and death between one and two hours. Sample I of the seed was used in only one experiment, and in that case was more toxic than sample II. It occurred to me that this might be due to a difference in the toxicity of green seed as compared to ripe, for, owing to the method of collecting it, sample II contained more ripe seed than sample I. Fortunately, although it was late in the year (May), I was able to procure locally sufficient green berries to put the matter to a test. At first it seemed impossible without serious loss of time to mechanic- ally separate the small unripe seeds from the green fleshy petals, and after separating enough to find the percentage of seed present (18-2) the whole unripe fruit was administered in the form of a watery suspension. This gave the following results : 27 grm. fruit per kilogram caused death in forty-five minutes; 14-4 grm. in ninety-five minutes; 10 grm. in two hours and a half. As 10 grm. fruit contained only 1-8 grm. seed, it followed that either the unripe seed contained a very large amount of tutin, or that, at this stage, it was also present in the fleshy petals. To decide this point it was necessary to obtain a clean sample of unripe seed, and after several attempts the following method was found to be successful : Berries were dried in air at a mode- rate temperature and ru.bbed between the fingers ; by this means the seeds were isolated from the remainder. The material was then put. 4 Transactions. in small quantities at a time, mto a mixture of naphtha and chloroform of such a specific gravity that the seeds floated while all the dehris sank, and by skimming off and drying the seed a fine clean sample was obtained. When administered to a rabbit this gave the result shown in the table, exp. 296 — viz., the percentage of tutin was no greater than the average. It follows, therefore, that at an early stage in the forma- tion of the berry the fleshy petals contain as much tutin as other green parts of the plant — in fact, the percentage works out to the same (0-06) as was found m the green shoots of Goriana ruscifolia. It would be interesting to be able to follow the fate of the tutin in the petals. Is it transformed in situ into a constituent of the innocuous juice, or is it transported to other parts of the plant ? If the former takes place, one is tempted to believe a ferment might be found capable of affecting the transformation, and such a ferment would be of value in destroying tutin while still in the paunch of stock poisoned by tutu. So far I have not been able to get any evidence of the presence of such a ferment. Effects of .\dministeation of the Oils. Practically all parts of the tatu-plant, but especially the seeds, contain a considerable amount of a green-coloured oil — " oil of tutu " — which was believed by the earlier workers (Skey, Christie) to be or to contain the poisonous principle. That the latter supposition was the correct one was proved by Easterfield and Aston, who showed that tutin, quite apart from the oil, was sufficiently active and abundant to account for most, if not all. of the symptoms of tutu poisoning. The question still remained, however, whether the oil or oils had any action which if not toxic itself might influence the toxicity of the tutin. To throw some light on this I used the oil as obtained by extraction v/ith mineral naphtha, which had proved itself a good solvent for oil, while it was unlikely to dissolve tutin, as this substance had been shown by Easterfield and Aston to be insoluble in benzene. Chloroform extracts were also investigated, because it was noticed that, after naphtha extraction had been carried on till the extracts were colourless, chloroform was still able to extract some green-coloured oil, probably another fraction of the mixture of oils present. The follow- ing experiments were done ; — {a.) 50grm. seed (sampL' 11) was extracted first with mineral naphtha till the extracts were clourless, then with chloroform. The chloroform-soluble part was mixed with a little alcohol and added to water, the result being a fine precipitate or suspens-iou of the oil. This was administered to a rabbit by stomach-tube. The animal became unconscious, and remained so for about three hours. Next day it appeared to be quite well. The symptoms were probably due to the dcse of alcohol, which unfortunately was not measured. No distinct tutin eSects were obsserved. {h.) A quantity of the oil extracted with naphtha was freed from all but traces of the solvent by heating it on a water bath ; some olive-oil was added, and a small amount of egg-white and 1 per cent, sodium carbonate. The mixture was then emulsified by shaking, and administered by stomach-tube. No symptoms developed beyond r -me somnolescence. The amount of green oil given would amount to about 10 grm. = 8 grni. per kilogram for the rabbit used. (c.) 50 grm. seed (sample II) was extracted with alcohol, and the residue extracted with chloroform. A considerable amount of green oil resulted. This was boiled with about a litre of water, filtered, and evaporated down on a water bath. More " oil " continued to separate as evaporation pro- ceeded, and was removed by filtration. The final result was 10 c.c. of watery extract of the "oils." Of this 5 c.c. was administered by hypo- dermic injection to a medium-sized rabbit. No symptoms followed. Malcolm. — Toxicitij of Tiifu F>-uif a ml Sr-eJ. 5 (d.) 20 grm. seed (sample I), previously extraofced wibn uapiitha, was extracted with chloroform, which removed a further quantity of green oil. After driv- ing oE the chloroform the oily residue was extracted with 100 c.c. water, filtered, and concentrated to 10 c.c. Of this 5 c.c. given hypodermically produced no symptoms. The conclusion to be drawn from these experiments is that the oil, or oils, has no toxic action. It is probable that the chloroform extracts contained some tutin, for tutin is soluble therein to a small extent, but the amount was either originally too small to produce symptoms or it underwent destruction in making the hot-water extracts. Methods of extkacting Tutin. Although at present there seems little likelihood that the pure substance, tutin, will ever be of any therapeutic or other commercial value, it may be of use to workers on the subject to add a note on the methods of extracting it. The best source of tutin is the seed — ripe or unripe. Drying in the air probably does not lead to any loss, but crushing and grinding, especially when combined with watery extrac- tion and evaporation, lead to considerable loss. So far as my present experience goes, the best method is to extract the oils from the dried and recently crushed seed with mineral naphtha, and then extract the residue with ether. The ether-soluble material can then be again extracted with naphtha to remove more of the oils, and the result is an extremely toxic material, which can be further purified as described by Easterfield and Aston. Summary and Conclusions. 1. No evidence was obtained of any toxic substance in the juice of the ripe tutu-fruit. 2. The green petals of the unripe fruit contain as much tutin as other green parts of the plant. 3. Both ripe and unripe seeds contain between O'l per cent, and 0'6 per cent, of tutin, being about double what is found in young shoots in the natural state. (When the water percentage is taken into account there is not much difference.) 4. The constituents of the seeds soluble in naphtha and chloroform (oils and resins) were not found to possess any toxic action. 5. The sugars present in the juice of the berry appear to be a mixture of dextrose and laevulose. Eeferences. FiTCHETT, F., 1909. Physiological Action of Tutin, Trans. N.Z. Inst., vol. 41, pp. 286-366. (This pap^r gives a full list of previous work on tutin.) Malcolm, J.. 1914. Some Experiments on Tutin and Tutu Poisoning, Trans. N.Z. Inst , vol. 46, pp. 248-54. Transactions. Art. II. — The Significant Features of Reef-bordered Coasts. By W. M. Davis, Harvard University, Cambridge, Mass., U.S.A. [Read hejore the Wellington Philosophical Society, 16ih October, 1918 ; received bi/ Editor. 16th October, 1918; issued separately, Uth May., 1919.] In recognition of the honour conferred by the New Zealand Institute in adding me to its list of honorary members, and in return for the kind reception given me at its meetings during my Pacific journey in 1914, I desire to offer the following notes for publication in its Transactions, in the hope that they may aid students of coral reefs in observing certain features of significance in connection with the origin of those extraordinary struc- tures. References are appended to a number of my articles, the product of observation, reading, and refiection during five years past, where certain aspects of the coral-reef problem are treated more fully than they can be here. Sea-level Coral Reefs are silent as to their Origin. — The corals and other organisms of a sea-level reef are tru.ly of marvellous interest, and from a zoological point of view merit all the attention they have received ; but when a reef is examined from a geological point of view its organisms are found to be reluctant, not to say incompetent, witnesses as to the manner of its formation. An observer may sail along the front of a reef, wander over its surface, or row about in its lagoon, and discover many facts regard- ing the varied forms of life there visible, and regarding the processes, organic and inorganic, now in operation ; but, apart from such factors as the temperature and the depth of sea-water at which reef-building corals grow, he can learn little, if anything, about the past conditions under which the reef has been developed, so long as his study is directed to the reef alone. On atoll reefs there are, indeed, no facts visible at the surface by which the various theories of the origin of coral reefs can be tested : it is only from borings m sea-level atolls or from natural sections of elevated atolls that competent testimony as to their origin can be gained. In this con- nection it may be noted that the interpretation of the Funafuti boring recently published by Professor E. W. Skeats, of Melbourne (1918),* gives a much better statement of its evidence as to the origin of that atoll than is to be found in the original report published by the Royal Society, which was almost silent as to the meaning of the facts that it set forth so minutely. Fringing and barrier reefs are, on the other hand, associated with the coasts of land-masses, which may yield much information as to the past conditions and processes of reef-formation, if the geological structure and the physiographic development of the coastal slope are examined. For these reasons it is to the coasts of the land-masses which fringing or barrier reefs adjoin that attention is here chiefly directed. Coasts of EMERaENCE and of Submergence. The general features of coasts on which coral reefs occur — either fringmg reefs alone, or fringing reefs in the lagoons enclosed by barrier reefs — give helpful indications of the relative changes of level that the coasts have * For references see p. 30. Davis. — Signified ni Features of Ecef -bordered Coasts. 7 suffered. Some coasts have a smooth seaward slope, and consist of imperfectly consolidated marine strata, dipping gently seaward, which have been little eroded since their emergence from the sea in which they were deposited : these are typical coasts of emergence. Other coasts, whatever their structure may be, exhibit forms of subaerial erosion, such as hills and valleys, the slopes of which appear to continue below sea-level, as if they had been partly submerged since they were eroded : these are coasts of submergence. Coasts of Emergence. — Along coasts of emergence of the kind above specified the shore-line will generally be almost rectilinear or of simple curvature. The amount of emergence may be inferred from the altitude to which the marine strata rise along their inland border. It may be at once stated that coasts of this kind are seldom fronted by coral reefs, apparently because the loose sediments of their beaches and submarine slopes do not afford a suitable foundation for coral-growth : witness the Madras coast of India, the south coast of Java, and the west and south coasts of Borneo, all of which bear marks of sub-recent emergence. Another class of coasts of emergence, on which coral reefs abound, will be given special description below. Young Volcanic I.slands. — The coasts of young volcanic islands may be associated with coasts of emergence, especially if composed largely of ash and not of solid lava. They are frequently cliffed and beached, without reefs. Barren Island, east of the Andamans, in the Bay of Bengal, is some- what cliffed, and but little fringed with corals. Reunion, in the western Indian Ocean, has reached a rather mature stage of erosion and abrasion, with a very imperfect development of fringing reefs, as will be further explained below. It therefore resembles certain strongly cliffed volcanic islands in temperate latitudes. Let it be noted that the cUffs of such islands are usually cut back by the waves at a faster rate than the valleys are cut down by their streams, so that the valleys are left hanging above sea-level, and their streams cascade do^vn the cliffs to the beach. Coasts of Submergence. — On coasts of submergence the shore-line will necessarily be irregular, advancing seaward around the outstanding points of partly submerged spurs and entering landward around the branching embayments of partly submerged valleys. Conversely, shore-lines of this kind indicate that the coasts which they border have been submerged, as Dana pointed out in 1849. Singularly enough, Darwin never perceived the value of this evidence in support of his theory (Davis, 1913). The spur-ends of coasts of submergence in the coral seas usually offer excellent opportunity for the growth of fringing reefs, for their firm rocks are soon swept bare by the waves, and they are free from the detritus that accumulates in the bay-heads. If the submergence be slowly continued, a fringing reef, A (fig. 1), may be transformed into a barrier reef, B, by upward growth as the sea-level changes from S to T ; but if the sub- mergence be renewed at a more rapid rate, changing the sea-level from T to U, the barrier reef will be drowned, and, if a pause then occurs, a fringing reef of a new generation, G, will be formed, as will be more fully stated below. , Unconformable Reef Contacts. — In all cases of reefs bordering coasts of submergence the original fringing reef which forms the base of an upgrow- ing barrier reef, as well as the lagoon deposits within the barrier reef and the secondary fringing reefs that grow on the spur-ends of the lagoon shore, and also all fringing reefs of new generations, must rest unconformably on 8 Transactions. an uneven foundation of subaerial erosion. This point has been too gene- rally overlooked, although it is of the highest theoretical importance. Its converse is of practical value : reefs that rest unconformably on surfaces of subaerial erosion must have been initiated by submergence. Hence the natu.re of the contact of a reef and its foundation should be carefully observed, whether the reef be at sea-level or elevated above it. ^rrflMnit iiiii lin' Fia. 1. Amount of Submergence. — The amount of submergence that an embayed coast has suffered is not well indicated by the depth of its embayments, for they may be much filled w^ith sediments ; the amount is better inferred by drawing a true-scale cross profile, as at P. fig. 2, of the spurs that enclose a bay-mouth, and continuing their slopes with decreasing declivity below sea-level until they meet. The visible cross-section of the valley above the Fig. 2. bay-head at Q should be taken as indicating the pattern of the submerged cross-section at the bav-mouth, P. The measure of submergence thus gained is only a minimum value, for, as shown in fig. 2, the depth of the submerged valley near the bay-mouth may be only about half the depth of the original valley-mouth, \ . Pre-submeiyeuce Period. — The duration of the pre-submergence period of subaerial erosion should be estimated as short, long, or very long, by com- paring the actual form of the visible land-surface with its inferred initial form, due allowance being made for rock-resistance. In the case of dis- sected and embayed volcanic islands this comparison may often be made without much difficulty. On the coasts of continents and of continental islands the comparison may not be so easily instituted, but an attentive examination of the form of the coastal slopes will usually suffice to deter- mine whether the cycle of erosion was in an early, middle, or late stage of its progress when it was interrupted by submergence. Davis. — Signifiaaii Fta/iires of Rft f-lioi(h i-rd ('mists. 'J Thus the submergence of the Queensland coast, in association with wliich the Great Barrier Reef of Australia and the discontinuous fring- ing reef in the broad lagoon were formed, did not occur until the rather resistant rocks which there prevail had been reduced to subdued forms of late maturitv or even to the low relief of old age. The same may be said of much of the south-western coast of New Caledonia, except that the rocks there present near the shore are for the most part weaker than those of Queensland. In both these examples the pre-submergence period of sub- aerial erosion must have been of long duration. In view of these various considerations it is evident that careful obserxa- tion should be made of reef-bordered coasts from a physiographic as well as from a geological ])oint of view, in order to determine whether the reefs have been formed in association with the submergence or the emergence of their foundation. It is also important that reef-free coasts in the coral seas should be similarly observed, in order to discover the conditions that do not favour reef-forniation. Rate of Submergence. — The ordinary statement of Darwin's theory of coral reefs implies that the rate at which reef-foundations have been sub- merged as a result of their own subsidence must not be greater, but may be less, than the rate of reef-upgrowth ; and this has been held to be an improbable condition. Darwin's own statement of the problem made no such limitation as to the rate of subsidence, except where barrier reefs and atolls are actually found. For those reefs he stated that relatively rapid subsidences of small amount alternating with long stationary pauses pro- babl}' represent the ordinary succession of events, and he believed that the average rate of submergence thus determined was not in such cases faster than the rate of reef-upgrowth. This seems to hold true for the greater part of the open Pacific, where atolls and barrier reefs prevail, even though the submergence due to insular subsidence there has been accelerated by a sub-recent rise of ocean-level during the melting of the Pleistocene ice-sheets — a matter which has come into importance in recent years, as will be shown in more detail below. But exception to this statement is needed for an area to the north of the Fiji Group, where fifteen or more submarine banks, apparently submerged reefs or " drowned atolls,"' have been discovered since Darwin's time ; and also for the region of the Tonga Islands, where extensive submarine banks occur. In both these regions of the mid-Pacific, and in a few others, sub- mergence appears to have taken place at a faster rate than reef-upgrowth. They thus corresjjond to a large part of the Indian Ocean, where submarine banks, ap})arently " drowned atolls,'' prevail, as Darwin clearly understood. Darwin on Fringing Reefs. — Furthermore, although Darwin regarded most fringing reefs as having been formed on stationary or on rising coasts, he clearly understood that rapid subsidence might drown earlier-formed reefs, whereujjon the reefs that would grow on the new shore-line would be of the fringing class, as noted above. The statement of this point on page 124 of his Coral Reefs (1842) deserves attentive reading. True, inas- much as Darwin did not understand that embayed shore-lines and uncon- formable reef contacts around spur-ends are sure signs of submergence, he discovered no examples of fringing reefs of this kind in the records that he studied, and all the fringing reefs on his chart are classed as occurring on stationary or rising coasts. But his deductive expectation may now be confirmed, for the Austral- asian and other archipelagoes contain numeroiis examples of fringing reefs 10 Transactions. unconformably contouring around the spur-ends of embayed coasts — witness Palawan, the south-westernmost member of the PhiUppines, and many other embayed islands in that group — well represented in recent charts of the United States Coast and Geodetic Survey ; also the Andaman Islands, in the Bay of Bengal ; for in all these examples the coast is elaborately embayed ; and hence their fringing reefs must be unconformable, and their submergence must have taken place at a faster rate than reef- upgrowth. Many other examples of the same kind might be cited. Fringing Reefs and Submarine Platforms. — Fringing reefs thus assume a much greater interest than is generally allowed to them : their relations to the features of the coasts they border deserve close attention. The breadth of the reefs should be noted as a means of estimating the time that has elapsed since the last movement of submergence took place. The ofi-shore soundings of reef-fringed coasts of submergence are also of importance, for they frequently reveal a submarine platform that in all probability represents a drowned barrier reef and its lagoon. Such submarine platforms, several miles in width, are found in association with Palawan and the Andamans, although the sea-level fringing reefs of these islands are narrow. A well-developed submarine platform surrounds the greatly denuded " volcanic wreck " of Fauro, a small island with narrow fringing reefs in the Solomon Group. A similar platform is shown by the latest surveys of the United States Hydro- graphic Office to surround the Samoan island of Tutuila ; but the fact that the spur-ends of this island are rather strongly clified behind their fringing reefs distinguishes it from the other examples named. Submarine platforms occur around the Marquesas Islands also ; but here, although the spur-ends are cliff ed, as in Tutuila, they are not fronted by fringing reefs. The depth of the submarine platforms ofi reef-fringed shores is not constant : along the west coast of Palawan the platform varies in depth from 25 or 30 fathoms near its southern end to 60 fathoms near its mid- length ; the Fauro platform has depths of 70 or more fathoms ; the Andaman platform is 30 or 40 fathoms in depth. On the other hand, part of the coast of Samar, in the Philippines, facing the open Pacific, has fringing reefs around its headlands, but its submarine slope descends rapidly to great depths. Now, let it be noted, first, that the three chief elements of the fringing-reef problem as here considered — duration of the pre-submergence period of subaerial erosion, rate and amount of submergence, and duration of post-submergence period of fringing-reef growth — have unlike values on difl'erent islands ; secondly, that many other islands have well-developed barrier reefs which suggest slow sub- mergence, and that some barrier reefs are broad and others are narrow, thus suggesting that the rate and date of their submergence are unlike ; and, thirdly, that many elevated reefs occur at difterent altitudes and in different stages of erosion. It thus becomes evident that the history of various reef-encircled islands must consist of unlike sequences of movements and pauses. Hence local movements of the reef - formations themselves, which may varv greatly, explain the varied facts much better than changes of ocean- level, which must everywhere be of the same rate, date, and amount. In order to learn how greatly the values of the various elements differ from place to place, their value for every coast should be determined independently. One of the most important of these elements is the Davis. — Significant Feattires of liitf -bordered Coasts. 11 duration of the post-emergence or post-submergence stationary period, the estimation of which may now be considered in some detail. Time since Emergence. — The shore-line of an emerged and thence- forward stationary coastal plain may be locally built forward, or " prograded," by deltas if its rivers are of large volume and well charged with detritus from an elevated backland ; and sand reefs enclosing shallow or marshy lagoons may be cast up by the waves between the deltas, and may advance seaward as the delta-fronts advance. Conditions of this sort appear to prevail along the Madras border of India, and around the south-west side of Borneo, thus proving that these coasts have been somewhat changed from their simpler initial form ; but the littoral conditions are still manifestly unfavourable to coral-reef formation. It is conceivable, however, that after a temporary supply of gravel and cobbles has been washed out by a flooded river to a certain part of the front of a delta that is for the most part composed of finer sediments the river may change its course, as rivers on deltas are prone to do. Then corals, attaching themselves to the larger cobbles, may spread sufficiently to form a small fringing reef, until a return of the river buries the corals. A buried reef of this kind will slant forward with the delta-front, and will lie conformably between the earlier and later foreset delta-beds. Such seems to have been the origin of a small elevated reef near Suva, Fiji : it lies on a local deposit of gravel, and both the gravel and the reef lie conformably in the slanting beds of volcanic mud, there known as '' soapstone." The extent of the littoral lowland that is prograded along the border of a coastal plain will give some idea of the time that has elapsed since the plain emerged. But such lowlands are not always developed ; for, if large rivers are wanting, the shore-line of a coastal plain may be cut back or retrograded farther and farther by the sea, as long as no change of level takes place. The farther it is cut back, the higher will be the resulting bluSs along the coastal-plain margin. The height of the bluffs along the shore of a retrograded coastal plain will therefore give an indication of the time during which it has been attacked by the sea. A more important point is that, however far such a stationary coast may be retrograded, a beach of loose detritus, continued off shore by a sheet of finer sediments, will, according to accepted physiographic theory, always cloak the abraded ^^latform along the base of the retreating bluff's. No reefs are therefore to be expected on such a coast. The ReeJ-free Coast of Madras. — It is important that the coasts of the coral seas should be examined with these principles in mind in order to test their correctness. As far as I have read, there is no published account of a strongly retrograded coast in the torrid seas that is still suffering abrasion in its original stand with respect to sea-level. It is interesting to note, however, that the high, hard-rock cliffs which, as described by Gushing, rise a short distance inland on the coast of Madras appear to have been cut back by the sea before the emergence of the present Madras coastal plain ; hence the cliffs must, before the sub-recent movement of emergence by which a negative shift of the shore-line was caused, have exemplified a maturely retrograded, reef-free coast ; and at the beginning of their abrasion the hard-rock land-mass must in all probability have been covered, near its shore-line at least, with the sedi- ments of an ancient coastal plain of emergence, just as the emerged platform of marine abrasion which fronts the high cliff's is covered by a 12 Transactions. modern coastal plain to-day ; for otherwise it is difficult to understand why coral reefs should not have been formed there and have prevented the cutting of the high cliffs. cuffed Volcanic Islands. — It has been suggested above that the shore- lines of volcanic islands may be regarded as shore-lines of emergence, particularly if the island is largely composed of loosely compacted volcanic ash ; for such a shore-line will be of comparatively simple outline, without pronounced salients or embayments, and the detritus washed down its slopes by its streams, added to that cut by the waves along the shore, v.'iU soon form a continuous beach, extending seaward in a sheet of loose sediments, on which reef-building corals cannot attach themselves (Davis, 1916b). Under such conditions the island will be continuously attacked by the waves, cliffs will be cut around its shore while valleys are eroded in its slopes, and if the island stand still long enough it will be com- pletely truncated. Even then it may be difficult for corals to find a firm foundation for their growth until nearly all the loose detritus is swept off the surface of truncation. According to Admiral AVharton, atolls were supposed to have been built up around the margin of truncated volcanic islands, no change of sea-level and no subsidence of the island being postulated. Darwin had previously considered this possibility and rejected it, because the resulting lagoons would be too shallow. Ac rding to Daly, atolls are supposed to have been built up on volcanic platforms that were abraded while the ocean was lowered and reef-building corals were killed, during the Glacial period. The best test of these suppositions involves a series of borings along the diameter of an atoll to a depth of 50 or more fathoms below present sea-level : the elevated atolls of the Loyalty Islands are to be recommended for such examination. If it be true, as above suggested, that still-standing volcanic islands may, in the absence of protecting reefs, be cut away by the sea, a number of examples in different stages of abrasion should be found in the coral seas of to-day. Reunion is the best example of the kind, stiU in process of abrasion, that has come to my attention. Tahiti is an equally good example, but it has been somewhat submerged, and its shores are now defended by coral reefs, as will be more fully described below. Tutuila, in Samoa, and the Marquesas Islands probably, as noted above, belong to this series, biit their place cannot be safely determined at present. Most volcanic islands in the coral seas are surrounded by barrier reefs, and their shore-lines are not cliffed. It is very desirable that aU islands of the coral seas should be examined with the points here set forth in mind. The brief accounts now available of many such islands do not suffice to determine what stage of erosional and abrasional evolution they have reached. Time since Submergence. — The headlands of coasts of submergence in temperate latitudes, not being defended by coral reefs, are vigorously attacked by storm waves ; thus a cliff is formed rising high above sea- level, and a platform lying a little below sea-level. Coasts of submergence in the coral seas are as a rule fronted by barrier reefs or bordered by fringing reefs ; hence they do not generally show the strongly cliffed spur- ends that characterize similar coasts in temperate latitudes. True, the spur-ends of such coasts are often cut off in low bluffs, B (fig. 4), 10 ft. to 50 ft. in height, forward from which one may see low-tide rock platforms 30 ft. to 100 ft. in breadth before one reaches the fringing reef, F, that is ordinarily found in such situations. Davis. — Si(jii ificnnt Ftafurex of l\nf-li(>ilfif^- ^X^='l^-'-^''^l>S-- m " 'W^^^ ' "/s~'^^Ok- '-^^ w^Jl^p, 8 Fig. 6. — Peneodrilus durvilleanus. Spermatheca. The dotted circles on the diverticula indicate the chamberlets, which are visible only when the organ is cleared. Fig. 7. — P. durvilleanus. The left side of segments 8 and 9, showing the spermathecae, nephridial tuft and its lateral extension, and in the latter segment the sperm-sac (s). The median line is towards the right side. Fig. 8. — P. durvilleanus. The left half of segments 12 and 1.5, showing the gradual dissolution of the nephridial tuft and its extension dorsalwards. and left sides of the ampulla (fig. 6). Externally they appear simple, but when mounted and viewed as transparent objects the internal chamberlets are visible. In this condition the diverticulum appears as a semicircular collar round the duct, much as I have figured it for P. ricardi (5) ; but seen in the animal the distinctness of the two long processes of the diverticulum is very evident. There are four pairs of sperm-sacs, in segments 9, 10, 11, 12. The two anterior sacs have at present the form of long white slender cylindrical tubes resting against the hinder septa of the segments (fig. 7) ; each terminates upwards in a rounded end, and is attached ventrally to the septum close to the body-wal- and nerve-cord. The two posterior sacs are shorter, wider, and lie along the anterior wall of their segments (fig. 8) : in short, they have the usual position, but are at present only commencing to form. 40 Transactions. The Nephridia. — From the 2nd to the 14th segments, inchisive, the nephridium is represented by a conspicuous tuft of minute looping tu])ules arranged in such a way as to form a sort of " rosette " close to the nerve- cord and occuj^ying nearly the whole length of its segment. It is thus a more or less rounded or quadrate mass of tubules. These tufts are much larger in the more anterior segments, and in the 2nd, 3rd, and 4th seem to represent the entire organ, but farther back one sees that the tubules are not confined to these tufts but extend outwards along the body-wall for a short distance as a linear series of isolated loops near the septa (fig. 7). In about the 7th-llth I believed that under a high- power dissecting-lens I could detect a duct or tube passing outwards, and ending apparently on the body-wall about half-way up the side of the body. I therefore cut out, stained, and mounted a portion of the side of the body, including the segments 7-11, in the hope of being able to satisfy myself as to the locality of the pore ; but I was unsuc- cessful. The body- wall is too soft to allow such a small aperture to be recognized. I then mounted the cuticle of these segments, but was no more successful, for, though the large spermathecal pores and the linings of the chaetiferous follicles are perfectly evident, there is no pore that I could interpret as being the nephridiopore. Sections were equally useless, owing, as I believe, to the soft condition of the specimen. To continue the internal appearance : The dissolution of the tuft of the tubules, which commences about the 7th segment, continues till at the 15th almost all the loops are arranged in the linear series (fig. 8), and by the 17th I fail to see any tuft or rosette. At the 20th I am unable to detect any loops under a lens, but by picking up at random the tissue that lies between the septa I find under the microscope that it consists of minute nephridial tubules with accompanying blood-vessels. I was unable to detect any funnel, but the poor state of the tissue has rendered it difficult to make as thorough an investigation on this important point as is necessary. However, it is clearly, 1 think, a " meganephric " worm such as I have previously described. Locality. — D'Urville Island. Remarks.~The genus Perieodrilus (which Michaelsen has separated from my Plagiochaeta) (4) is so far confined to the mountains of the West Coast : it is therefore not surprising that a representative occurs in this island. It is evident that the present species is nearly related to P. montanus and to P. ricardi (5), but from each it differs in one or more features. Externally its coloration recalls that of the former, as also in the con- centration of the nephridial loops near the ventral region of the body (6) ; but in P. montanus the gonads are situated on the posterior wall of their segments, in P. ricardi they are on the ventral wall midway between the septa. Only in P. lateralis are they in their normal anterior position as in the present species, but in that worm there are no oesophageal glands and only two pairs of sperm-sacs. In the two other species, while there are four pairs of sperm-sacs, there is only one pair of oesophageal glands. The form of the spermathecal diverticulum Hkewise differs from that in the known species. Benham. — hearth irortns from Stephen Islaiul and D'Urvillf Island. 41 References. 1. W. MiCHAELSEN, Oligocli. V. d. Inselii des Pacific, Zool. Jahrb. (System), vol. \2, p. 230, 1899 ; and Ude (2), p. 413. 2. H. Ude, Terricole Oligoch. v. cl. Inseln d. Sudsee, u.s.w., Zeit. fur M'iss. Zool.. vol. 83, p. 4(t5. 1905. 3. F. E. Beddard, On some New SiDecies of Earthworms, &c., Proc. Zool. Soc. Lomlon, p. 671, 1892. 4. W. B. Benham, Notes on two Acanthrodriloid Earthworms from New Zealand, Quart. Journ. Micr. ScL, vol. 33, p. 289, 1892. .5. W. B. Benham, On the Old and some New Species of Eai'thworms belonging to the Genus Plagiorhaefa, Trans. N.Z. Inst., vol. 35, p. 277, 1903. *i. W. B. Benham and G. Cameron, The Nephridia of Ferieodrilus. Trans. N.Z. Inst., vol. 45, p. 191, 1913. Art. V. — :0n the Occurrence of Three Bands of Marble at South Peak, near Hampden, Otago. By Professor James Park, F.G.S. {Read before the Olacjo Institute, 10th December, I'JIS ; received by Editor, 27th December, 1918 ; issued separately, lith May, 1919.] In the early part of last November, while investigating the extension of the Shag Point beds to the landward side of Hampden, I was informed by Mr. A. Craig, of that place, that an attempt had been made some twenty years ago to burn limestone in a kiln somewhere near the upper end of Baghdad Road. As the result of two days' search, with the assistance of Mr. Craig, I found a small outcrop of a grey crystalline limestone on the north side of Skinner's Creek, at an altitude of 450 ft. above the sea, at a point about 300 yards from Baghdad Road. The outcrop had been opened out by blasting, and I concluded that this was the place from which the material for the ex- perimental burning had been excavated. I con- tinued the search towards South Peak, and suc- ceeded in discovering three well-defined bands of limestone, two on the south side of Skinner's Creek and one on the north. These bands are interbedded in the altered argillite that forms the core of the coastal range lying behind Hampden. They strike almost north and south (true), and dip east at angles that vary from 50° to 65°. Band A is about 5 ft. thick ; band B, 12 ft. ; and band C about 2 ft. Bands B and C are separated from one another by 32 ft. of argillite. Band A, geologically the lowest, is perhaps 200 ft. below band B. J4-00 20 > 40 I 60 ^ycciJe ^f chains . ®Smilk P^nJc A, B, and C, lenses of limestone. 42 Trcnisacfions. When traced along the outcrop the limestone bands are found to occur as short lenses. Band A is a lens about 450 yards long, and bands B and C peter out in a distance of 70 yards. Like the blue crystalline limestone at Dunback, the Hampden limestone bands occur in the semi-metamorphic rocks of the Kakanui series of Hector, the age of which is still unknown. The relationship of the Hampden and Dunback limestones can be determined only by a detailed survey. The Hampden limestone is a fine-grained grey marble of good quality. The larger blocks will form good building-material, and the small pieces may be utilized for grinding into material for agricultural purposes. An average sample of marble from the lens marked A on the accompanying sketch was analysed at the Dominion Laboratory, Wel- lington, with the following results : — Insoluble in acid . . . . . . . . 0"86 Alumina and iron oxide . . . . . . 0'55 Magnesium carbonate . . . . . . 0"56 Calcium phosphate . . . . . . . . 0"17 Calcium carbonate (CaCOg) by difierence . . 97*86 100-00 I am indebted to the Director of the Geological Survey for obtaining the above analysis for me. Art. VI. — A Preliminary Investigation of the Age and Manner of Growth of Brown Trout in Canterbury, as shown by a Microscojyic Examination of their Scales. By M. H. CtOdby, M.A., B.Sc. {Read before the Philosophical Institute of Canterbury, 4th September, 1918; received by Editor, 20th September, 1918 ; 'issued separately, 14ih May, 1919.] Plates I-VL The possibility of determining the age of fish by a microscopic examina- tion of their scales was first demonstrated in 1899 by Hoffbauer (3), who made a special study of carp-scales. The same principle was applied to salmon-scales by Johnston (4) in three papers published in the 23rd, 25th, and 26th Annual Eeports of the Fishery Board for Scotland. Johnston further demonstrated that it was possible to trace the whole life-history of a salmon from its scales, and to say with tolerable certainty how long the fish had spent in fresh water as a " parr," at what age it had become a " sniolt " and migrated to the sea, whether it had re-entered fresh water to spawn, and, if so, the approximate dates of its re-entries and returns to the sea. Working on the same lines, Dahl (1) made a most careful study of salmon and trout scales in Norway, and showed that, in addition, it was possible to calculate with considerable accuracy the length attained by the fish each year of its existence. The fundamental fact on which these investigations are based is that carp, salmon, and trout — and, indeed, most if not all kinds of fish — each year GoDBY. — (jfroirfJi of Broini Trout in ('a/iferburi/. 43 pass through a period of rapid growtli followed by a period of comparative stagnation. This periodic growth has generally been attributed to changes of temperature and corresponding changes in the abundance of food-sujiply ; and in regard to many species of fish it has been demonstrated that the maximum rate of growth roughly coincides with the maximum temperature of the water. There is evidence, however, to show that this periodic growth is well marked in the scales of some deep-sea fish, which can hardly be subject to any marked seasonal changes of temperature, and in the case of the squeteague {Cynoscion regalis) Taylor (6) has shown that the period of stagnation roughly coincides with the spawning season in midsummer. It seems probable, therefore, that the period of stagnation is determined more by a voluntary fast during the spawning season than l)y any actual shortage of food, and that individuals which have not arrived at sexual maturity subject themselves to this annual fast, though not to the same extent as the mature specimens. This voluntary-fast theory is further borne out by the observations of Masterman (5), who in a most careful critic|ue of the previous work on salmon points out that a certain number of salmon captured at sea throughout the summer show no evidence of summer feeding. He concludes that some salmon start their spawning- fast many months before entering fresh water. This may cause the age of salmon to be underestimated in some cases, and certainly throws grave doubt on Johnston's claim that he can tell approximately the month of entering fresh water. In the case of trout there is no evidence of prolonged fasts, except during the spawning season, which occurs in midwinter, and it is of little importance whether the cause be lack of appetite or lack oJ' food. There is some evidence to show that in Canterbury the u\aximum rate of growth, especially amongst the larger fish, occurs in spring rather than in summer. It is probably quite safe to assume, however, that the period of stagnation occurs in the winter. Roughly speaking, a trout-scale (Plate I, fig. 1) consists of a transparent plate of more or less elliptical form, having its centre of growth approxi- mately at one of the foci. Surrounding this and roughly concentric with the outer edge of the scale are a number of lines or " circuli." The scale grows by the addition of these circuli round the periphery, which are added in greater numbers and more widely spaced during the periods of rapid growth. This alternate spacing and crowding produces light and dark zones, one light and one dark corresponding to a complete year's growth. The dark zones are called "' annuli," or " winter bands." In the case of spawning fish the stagnation is more complete, and the winter band is narrower and more clearly defined. In salmon (Salmo salar) the act of spawning leaves a clearly defined scar or " spawning-mark " on the scales, due to disintegration or reabsorption of the scale, especially along the lateral edges and the outer surface containing the circuli. A true spawning-mark is not very common in trout, but the character of the winter bands gives a fairly reliable indication of spawning. Plate I, fig. 1, shows one such winter band. The exact cause of the spawning-mark in salmon is still in dispute. Johnston (4) attributed it to the vicissitudes of river life, whereby the fish shrank in girth, and says, '" The compression of imbricated scales tends to increase the amount of overlap, and from this or dermic influences we find that their margins become ragged or frayed." Masterman (5) has shown that this fraying or erosion in many cases starts long prior to the fish's entry into fresh water, and concludes that the phenomenon is one of 44 Transactions. '■ erosion or absorption by the living tissue which is known to envelop the scale." Two possible explanations are suggested : " The process may be an anticipatory reduction of the size of the scale to meet the approachin» reduction in the girth of the body, or it may be connected directly with the formation and development of the ova." In Canterbury the spawning-mark is by no means so uncommon in trout as it appears to be in England and Norway. With male fish of con- siderable size (say, over 24 in.) it is rather the exception to find scales that do not show a definite spawning-mark — at any rate, in the Selwyn River (see Plate III, fig. 2). In females the act of spawning seems to leave a less decided scar, and most of the cases come within the region of uncertainty mentioned by Masterman, and introduce the personal element. In handling a large number of spawning fish this year, whilst collecting scales, I found that I could in almost every case detect the males by the texture of the skin. The males had a thick tough outer skin, and great difficulty was experienced in removing the scales, whilst no such covering was present in the females, and the scales were easily removed. Under the microscope the scales themselves were in many cases readily distinguished, those of the males being very much more eroded than those of the females. The ripe testes form a very much smaller proportion of the total weight of a male than the ripe ova of a female, so it is natural to suppose that the wastage of tissue in producing the former would be less than in producing the latter, and the shrinkage in milting is certainly less than in spawning, yet the scale-erosion is greater in males. All this seems to suggest that scale- erosion at spawning-time, in trout at any rate, is intimately connected with the production of the thick tough skin assumed by the males. Dahl has noticed that the erosion of scales in spawning salmon is more pronounced in the males, but apparently attaches no significance to his observation. In many cases it is a matter of opinion whether there is a spawning-mark corresponding to any particular winter on a trout-scale, but of the thirteen tagged fish from which I have scales every one shows, if not a distinct spawning-mark, at least a sharply defined winter band, such as the third winter band in Plate I, fig. 1, corresponding to the winter when the fish was stripped and tagged. I think it is probable that such winter bands are tolerably reliable evidence of spawning, but there is an almost perfect gradation from the broad ill-defined bands of the first two winters in Plate I, fig. 1, and many cases must always remain doubtful. Dahl (1) assumed that the scales grew in the same projiortion as the fish, and consequently that the distances from the centre of growth to the successive winter bands would be m the same ratio as the lengths attained by the fish in each successive winter. This assumption was almost in the nature of a corollary from what was previously known of the formation of winter bands, but experimental proof was desirable. Dahl and others have collected such a wealth of indirect evidence in favour of this hypo- thesis that there is little danger in accepting it as the basis of my investigations. Direct evidence, however, is difiicult to obtain, and is- meagre. As the whole of the present investigation depends on the truth of Dahl's hypothesis, it will be as well to add my small quota, more especially as Masterman and others have raised the objection that direct evidence is almost, if not entirely, lacking. The North Canterbury Acclimatization Society annually strips a number of trout in the Selwyn River for piscicultural purposes, and takes the opportunity to tag two or three hundred fish each year with a small silver GoDBY. — Growth of Brown Trout in (Janterhiiry . 45 label bearing a distinctive number ; at the same time particulars of length, weight, and sex are recorded. Through the kindness of the society, and of anglers who have had the good fortune to recapture tagged fish, I have secured scales from thirteen of these fish when recaptured, and have calculated from these scales the length of each fish when tagged. The following table shows the length when recaptured ; the length {a) actual, measured at time of tagging, and (6) calculated from the scales ; tosether with the difference in each case between the calculated and the measured lengths : — Tagged Length. Log No. Tag. No. Lens;th when ^Difference. recaptured. (a) Measured. (6) Calculated. Inches. Inches. Inches. Inch. B 25 1101 2U 191 20 \ B 26 1074 21 20 19f i B 27 1037 21 20 191 \ B 28 1088 221 20 20 0 B 136 1374 23 211 21i 0 BUT 1401 28 27 271 I B 159 1398 21 20 20 0 B236 1095 211 19 19i 't ' B246 1352 221 21 21 0 B 2.53 1346 221 21 21i 1 4 B277 1428 201 19 18f i B278 1380 221 21i 21f 1 B284 1304 21 19 m 'i r In no case is the difference between the calculated and the measured length more than ^ in., and in only three cases is it so much, whilst in four cases the agreement is exact. Considering the difficulty of measuring two or three hundred live fish accurately, these results may be taken to fall well within the limits of experimental error in measuring. In practice the fish are generally measured to the nearest i in., and an error of j in. at time of tagging and another J in. when recaptured would be sufficient to account for the largest discrepancy of h in. Two scales taken from one of these fish (tag No. 1374) at different times are shown (Plate II. figs. 1 and 2). The scale in Plate II, fig. 1, was taken on the 17th June, 1917, when the fish was tagged, and measured 21| in. The scale in Plate II, fig. 2, was taken on the 28th October, 1917, when the fish was recaptured, and meavsured 23 in. The lengths each winter, calculated from a set of scales taken in June and a set of scales taken in October, are as follows :— - Winters 1 J 2 3 1 ! i 4 5 (i 7 June scales (inches) . . 5 October scales (inches) . . ' 4^ 8* IH i7i 14J 17 19i 1 2U* 19 2l| 23* * Actual measured length. 46 T runsactions. Two fairly well-defined spawning-marks are shown in Plate II, fig. 2, and the space between the outer spawning-mark and the edge of the scale represents the growth of the fish between June and October. This growth (1| in.) certainly appears large as against 2^ in. for the whole of the previous year. It seems, however, to be a pretty general rule that the most vigorous growth takes place in the spring, and very little after midsummer, except perhaps in quite young fish. It should also be noted that the posterior end of this scale is well developed. This is usually a characteristic of vigorous growth, and this portion of the scale is usually the first to be eroded when deterioration sets in. It has been objected that scales are not permanent, but are shed and replaced by new scales. There may have been something in this objection until Dahl pointed out that scales with the so-called " expanded centre of growth " were in reality " replacement scales,'" and supplied the con- necting-link in a drawing of a scale which had been displaced in its socket but not actually lost. Plate I, fig. 2, shows a particularly fine example of such a " displacement scale," and is of itself almost convincing proof that normally scales are retained throughout a trout's life, and grow with the fish by additions round the outer edge. The Matekial. The material examined consists of three samples comprising respec- tively 33, 140, and 65 fish taken from the Selwyn River on the occasion of the annual stripping by the Acclimatization Society in 1915, 1917, and 1918 respectively, and smaller samples from several other rivers and lakes. I shall deal with each separately. Selwyn River. Table I (A) gives the complete figures for thirty-three fish, all males, stripped in the Selwyn in June, 1915. The scales were collected by Dr. C. Morton Anderson, who kindly handed them over to me. It is interesting to note that these scales had been simply folded up in paper for nearly two years when I received them, and had not deteriorated during that time. The second parcel of scales was taken by myself on the 17th June, 1917, and consists of scales from 140 fish, all being females except one, a particularly large male weighing 10 lb. The full figures are given in Table I (B). The average growth-curves are shown in fig. 1. The curve for the 1915 fish is a broken line, and that for the 1917 fish a continuous line. On the same diagram are also shown the curves for 173 fish from Lake Mjosen, in Norway, plotted from figures given in Dahl's book. The broken line again is the curve for males, the continuous line for females. In each case the males continue vigorous growth for a longer period than the females, and eventually outstrip them. As the males were from fish taken in 1915 and the females from fish taken in 1917, I thought it desirable to test this apparent difference between the sexes further, and with that object col- lected scales from twenty-nine males and thirty-six females at the annual stripping this winter (1918). The full figures are given in Tables I (C) and I (l5). The average growth-curves are shown in fig. 2. Again the raales continue vigorous growth longer and attain a greater size than the females. GoDBV. — G'ruivf/i (jf Blown Troiif in Canterhmn. 47 ' ^^ ^' ^, y ,, 30 _^'' y ^ y y — " y y !S y ^ y zs y / y ^ •' '■'"/ eo ^ '^■wvN so -^ *> g.U^'^J_- - // - f<> ■ — " ^ < yy.^ „ ," ^ ' ■''t'' /y yv // / // y ^y .y^ /<> y y ^ Z' .^ , X ^^ y^ ^ 6 J ^ /y /. // ^ J- ^ /^ ^o^^ ' p ^^ o Fig. 1. J* i A? „ 50 **5 ^l — — — zs ?f , --" 7f ^^ . — ■ — zo . BO t9 IS 17 to /S /♦ /J /^ / — y ^ — ^ y' ^ J ' ^ c / / / / / // // /o 9 a 6 S t 3 // y / X / / / / / o /. n Fig. 48 Transactions. From the AccUmatization Society's records I have calcrJated the average length of the fish tagged each year since 1915. The figures in parentheses give the number of fish measured : — 1915— Males, 20-8 in. (100) ; females, 20-1 in. (98). 1916— Females, 19-3 in. (199). 1917— Females, 20-4 in. (140). 1918— Males, 22-6 in. (66) ; females, 21-5 in. (156). In the years 1915 and 1918, when both sexes were tagged, the males averaged about 1 in. longer than the females. The average lengths of the samples from which I took scales are as follows : — 1915— Males, 21-3 in. (33). 1917— Females, 20-4 in. (140). 1918— Males, 22-5 in. (29) ; females, 21-7 in. (36). These figures agree closely with the averages for the total fish measured, so the samples were in all probability fairly representative. The year 1918 was remarkable both for the number and large size of the spawning fish. The average ages [see Tables I (A) to I (F)] indicate that the males either have a shorter life, or cease to run up the river at an earlier age. This bears out the general belief that the spawning mortality is greater amongst the males. .w in V 1$ 25 £9 7t ST ?•; ?i ^^^^ eo f» 19 il IS /5 f* /3 ?o ^■^ ^ / / / f^ r / / ^^ A „ ^ fO ■^ / 10 9 tt 7 y / / / / . f t '' / ■T ^ s S ^^ » // /X // ^ J o Fig. 3. A point to notice in these curves is that they are nearly straight lines for the first four years. This does not mean that each individual fish increases in length by approximately the same amount each year up to four years old. So far as my experience goes, growth of this character is almost unknown amongst trout in Canterbury, although such apparently is not the case in Norway. In Canterbury I have found that unless some outside influence is at work the rate of growth almost invariably starts to decrease quite appreciably in the third year, and this decrease is Trans. N.Z. Inst., Vol. LI. Plate I. Mfi^ pec 22 -JO l~~ r-t 1-^ S ^ .^ f-i cS o -*j > fS ^ t s o cS cc ■;;3 -B a; 'V* h-H ? g >. 3 "* H-H n _C ® le o o CI M T ;; 0+ -t^ f-* •+-J C p O o -4^ -5 ? a; o ,^ 1 — 1 w 1 ^- ! o 6 1 — 1 l-H if'ace ]>. 4S.] Trans. N.Z. Inst., Vol. LI. Plate II. CN O o ■? W — 'CD 1^ — l-"^ _ ■■— '— — .s '^'^ w -H t^ o 1* ^ o -Z. o ^ X 0 ^^ CI a. ^ tT ^ -4-i t^ .:: o 1 2^ " r -»-i > i'l f-J-i ^ ^^ ^ > *' ^ p- M ^ o; o ^ •». ^ o M ^ +3 ^ >i Pi =s s » Si)>.^ .\ o r-^ ^ 4^ • ^ o , ^ --^.■M r^ S 'V: f— ' ■^ *P 'M . .. .^ "~ CI *^ i*-- o ? - O ^ c "ti "k 3 6C P ' — ; ? '-^ C ^t~^ n 1 1 P? M HR Trans. N.Z. Inst., Vor.. LI. Plate III. mMw' "^>^».. '\ OJ ffi IS t; o ;_^ Oj .^ ce ^ i> fi ■-(-( o cj -fci ctf " a -^ '-' r^ tiiD g ■g fc/i Q M ■g r^ > ^ ' — ' 3 7. ^ r; ;^ ■ ■ Q rH > ■ -H --^i ■■^ •.C -n ^ - "* g .^ (~- bf) — tt '"" .;;3 •M VI & • •^ ci re ; v» — ^^ -^ ^~ . ^ 2 f- ^ ^ o ^ 0 p ?Q ?^ -; 'm' d 3 Trans. N.Z. Inst., Vol. LI. Plate IV. OJ c « I— I o ,2, o cS o O T3 ■? ^ ^ o QO ^ o .i-. o r-^ 01! Ci 1— 1 *. h-1 ..^ ■-^ 00 c5 C 02 ^ cS C^ C3 rr, tol C>) s ;h ^ o o > -t^ K .^ p^ -^ ' .^ -.-^ 02 P^ S P '^i V be - f^.^ cc ■> ^= _^,^_"o , 1 ,-t oi 0+ Tjf g ? — :::;'? <^ O C ^ C ^ GoDBT. — Growth of Brouui Trout in Canterbury. 49 more marked in the fourth year. A close examination of the figures in Tables I (A) to I (F) will show that in practically every case there is one year for each fish in which it has made more than normal growth ; it may be the second, third, fourth, or fifth year, but in almost every case there is this break in the growth-curve. This sudden jump or break is generally attributed to migration to more favourable surroundings, and there is every reason to believe that this is the case with the Selwyn fish. Practically all the spawning in the Selwyn takes place in the shallow, shingly part. Except in the spawning season, fish of any considerable size are rare in this part of the river. The traps are set just about the junction of the shallow water and the deep, to catch the fish working up to the spawning-beds. Consequently every fish caught has come from the deep water. Probably every fish was hatched and spent its early youth in the shallow part of the river ; therefore at some period it must have migrated to deep water. An examination of its scales will generally disclose when that migration took place The average curves, therefore, are really compounded of a number of different curves representing one-, two-, three-, four-, and possibly five- and six-year-old migrants. In fig. 3 are shown typical curves for a two- year-old and a four-year-old migrant. Plate III, figs. 1 and 2, show scales from these fish respectively, in which the period of better growth subsequent to migration is very distinctly shown. Whenever an average growth-curve closely approximates to a straight line for four or five years it is a fairly definite indication that the fish from that locality are migratory. Table I (E) shows the figures for thirteen trout caught last summer with rod and line at the mouth of the Selwyn and other streams running into Lake Ellesmere. The average rate of growth is about the same as that of the 1915 males, or intermediate between those of the 1918 males and females. In order to ascertain whether results in any way reliable could be obtained from smaller samples I calculated the average growth for the first, second, third, &c., twenty fish in Table I (B). Considering the very complex nature of the water, the agreement is quite satisfactory, and indicates that results. of some value can be obtained from quite small samples. Trout in the Selwyn, whatever the mode of growth, seem to have a more or less fixed limit of growth at about 23 in., which is rarely exceeded. Other waters also seem to show a maximum size-limit. It is curious, however, that this limit is occasionally considerably exceeded, and not necessarily by very old fish. These abnormally large fish, so far as I can ascertain, show no peculiarity of growth common to all, but their scales seem on the average unusually broad in proportion to their length, though I am at present unable to state this definitely. Whether the large size is determined by heredity or by unusually favourable environment I cannot say, though I am inclined to attribute it to the former. It is certainly a point worthy of further investigation. Particulars of five of these abnormally large fish are given in Table I (F). Rivers. From the angling point of view the rivers of Canterbury may be divided into two classes — snow rivers and rain rivers. The former contain large trout, for the most part, of sea-going habits ; the latter comparatively small trout, which are not as a general rule migratory. 50 Transactions. The material which I have examined up to the present consists of a quite inadequate number of fish from several rivers of each class. In Table II particulars are given of thirty-five fish from the Cam, North Branch of the Waimakariri, Styx, Selwyn No. 2, Opihi, and Tengawai, all of which I class as rain rivers. There are individual dift'erences, but the average rate of growth in all these is very similar. The average for the whole thirtv-five fish is — Winters 1 2 3 4 5 6 Inches 4-6 9-0 12-0 13-7 14-7 17-7 In Table III particulars are given of nineteen fish from the Ashley, Waimakariri, and Rakaia. The figures for the Ashley and the Rakaia agree very closely, but the figures for the Waimakariri are nearer to those for the rain rivers. The probable reason for this is that four out of the seven fish were taken from the Belfast branch of the river, which is frequently very low, and probably contains only a small percentage of sea-going fish. The average for the whole nineteen fish is — Winters 1 2 3 4 5 6 7 8 9 Inches 4-7 9-7 14-3 1 17-1 19-7 21-1 19-5 21-5 22-7 ^1 ^ J ♦ f i 7 » s ,e 1 f^ -- i- ^1 ^^ ^^ » " "i . " £3 ^^--^ .^ -' ,^ ^^ — "^ ■^ — ^ ..,- eO _^ " ^^ -' „ .'" :, • ' ^ -, .. ^ X '^ ,^^ /s r-' -^— -^ ' ^^ y ^^ 1-= ■/ ^ „ /o f / ^ /^ X y^ // - y ^■ yJ' s / s _/ / a / i / 0 / o Fig. 4. The averages for seven-, eight-, and nine-year-old fish are the figures for one fish only, an old jack from the Rakaia, which showed no sign of ever having been in the sea. The growth-curves plotted from these figures are shown together in fig. 4 for comparison — the rain-river fish by a continuous line, the snow-river fish by a broken line. The points to notice are that, although the rate of growth is approximately the same in each class for the first two years, the rain-river fish fall off GoDBY. — (jrrowth uf Broirn Trout in t'd/itt rbtiri/. 51 rapidly in the third, fourth, and fifth years, whilst in the snow-river fish a good growth is maintained. The growth-curve for the snow-river fish is a typical curve for a sample of which the individuals have migrated to more favourable surroundings at varying ages. Probably no individual fish has a growth-curve of this type, but the average curve is compounded of several different types representing the one-, two-, three-, and four- year-old migrants respectively. The sudden jump during the sixth year in the rain-river curve is the result of two fish only, and no importance attaches to it. It may seem rather arbitrary to include the Opihi as a rain river and the Ashley as a snow river. Each of these rivers is more or less on the border-line. Sea-going fish frequent each, and each contains a large number of small fish which have not been to sea, though possibly they may go later. It so happens that all my examples from the Opihi, which were caught in November, 1917, near the junction with the Tengawai, belonged to this latter class, whilst all the Ashley fish were largish fish which had probably been to sea. In view of the exceptionally poor growth of the Opihi and Tengawai fish, it would be most interesting to get scales from some of the large sea- run fish for which the Opihi is so famous, and to see whether these represent a later stage in the development of fish which as three- or four-year-olds had averaged only 10 in. to 12 in., or whether they belong to a different race. The matter is of some importance to the South Canterbury Accli- matization Society. If these poorly developed three- and four-year-olds are practically the " parr " stage of the larger sea-going trout the present con- dition of the Opihi is healthy ; if not, then in my opinion it is carrying a stock far in excess of its food-supply.* Plate IV, fig. 2, shows a scale from one of the Rakaia fish, and is an example of a very clearly marked scale, which is none the less difficult to read. The first winter band is clearly shown, and so is the second ; but immediately outside the latter is another darkening ; there is then a space indicating rapid summer growth, and the rest of the scale is normal. If this peculiarity existed in one scale only it might be attributed to some accident to or displacement of that particular scale. I have ten scales from this particular fish, and every one of them shows the same peculiarity. It has some meaning if one could only find it out. With some diffidence I offer the following explanation : The fish lived in the stream where hatched — probably the Rakaia — throughout the first year and the second summer and autumn ; when the second winter band was nearly complete it migrated to the sea, and immediately responded to the stimulus of sea- water. The stimulus, however, was short-lived, and winter stagnation again set in, causing the third check. So the second and third checks are really one winter band divided by a short period of rapid growth in winter, due to the tonic effect of sea- water. I have met this same peculiarity in one or two other fish from the Rakaia. Peculiarities such as this are not uncommon, and when they occur in one scale they invariably occur in every scale from the same fish, showing * Since writing the above I have received scales from two of the large sea-run fish of the Opihi, 26 in. and 201- in. in length. Tlie former ajjijears to have migrated as a yearling when about Gin. long, the latter as a four-year-old (jjossibly three-year-old) when about 10^ in. long. The early growth of this latter corresponds closely with that of the small Opihi fish previously mentioned. A scale from thi.s fish is shown in Plate IV, fig. 1. 52 Truasactious. that they are the result of some peculiarity in that fish's growth. Whilst very puzzling, these peculiarities are encouraging, for they open up possi- bilities for fresh discoveries in scale-reading. The Back-country Lakes. The material examined comprises ten fish from Marymere, fifteen from Lake Heron, three from Lake Coleridge, and two from Lake Alexandrina. Marymere. — The average growth in this lake is as follows : — Winters . . . . 1 2 3 4 5 6 7 8,9 ! Inches .. .. 5-4 12-6 1 17-2 19-7 21-5 22-7 23-4 24-2 24-4 The full figures are set out in Table IV (A), and the growth-curve is shown in fig. 5. The most striking feature of the curve is the large growth made during the second year, which exceeds even that of the first year ; and not only is this the case in the average curve, but it is true of every O ' « .15 1 1 ; 1 J« JJ ^0 Tf»' ^7 p$ ^5 ft SO /9 la a t6 1 — ■ ri ^ pfl ,, y /^ / / / J / fO / /a: 9 9 7 6 s 9 J / / / / 5 ' / / / / g / o Fig. 5. one of the ten fish examined, except one, in which the growth was equal for the first and second years. Such a state of aft'airs would generally be explained by saving the fish migrated at one year old to more favourable conditions. This cannot be the explanation in Marymere, as there are no streams running either into or out of the lake. It must be remembered, however, that the insects in our back-country districts are mostly large in size, and it seems probable that the true explanation is to be found in the fact that the main bulk of the food-supply is of a nature more suitable to fish after they have passed the yearling stage. Gilbert (2) has shown that quinnat and sockeye salmon which have migrated to the sea as fry a few months after hatching have very similar scales. GoDBY. — Growth of Hroivn T ront in C((iil( rhuni. 53 No brown trout have been liberated in Marymere since 1908, and so it is clear that they must breed in the lake itself, as three of the ten fish appear to have been hatched in 1914. It is curious that the next-youngest fish seems to have been hatched in 1911. In dealing with such small samjiles it is dangerous to generalize, but it certainly looks as if 1914 was an excep- tionally favourable breeding season. Plate V, fig. 1, shows a scale from one of these fish hatched in 1914, and Plate V, fig. 2, a scale from one of the older fish. The latter illustrates clearly the difficulty in determining" the age of old fish, owing to the way in which the winter bands are crowded together towards the edge of the scale. It is probable that the per- centage of ova hatched in Marymere, except in very favourable seasons, is abnormally low, and that the stock of fish is maintained mainly by the greater average age attained. Whether this latter is due to natural causes or to the limited amount of angling I am unable to say, but it is a characteristic not only of Marymere but also of other back-country lakes. The average age is 6-4, calcidated to last winter ; and as these fish would probably all have survived until next spawning season their average age would then have been 7-4 years, or about \h vears older than the Selwvn fish. Lake Heron. — The average growth is as follows : — Winters I 2 3 4 5 6 7 8 9 10 Inches 4-4 9-0 14-4 18-2 20-4 21-5 22-6 23-0 23-7 23-7 The full figures are set out in Table IV (B), and the growth-curve is shown in fig. 6 as a continuous line, the Marymere curve being reproduced If ^^ -J3 ^_ 30 n 16 25 — — -1 ^— — " — li ^_ - — " ^^J ' — ^ --' ^ ■ — 2& ^ - y n ' X 16 /5 /5 / X -' / > /^ / / ,1 / ^^ / X ,, ffl / /a 9 e f / ' / / / / / s 5 / / -'^ r // y ? y 0 /^ 0 Fig. 6. as a broken line for comparison. Although the size of the older fish approxi- mates fairly closely to that in Marymere, the average length of the younger 54 Transactions. fish is distinctly lower, especially at two, three, and four years old. It is also noticeable that the curve is nearly a straight line for the first four years, and that even in the fifth year the falling-oft' is not very pronounced. In dealing with the Sel'wyn fish I pointed out that a curve of this character was to be associated with a sample of fish containing individuals which probably migrated to more favourable conditions at varying ages. An examination of the figures in Table IV (B) shows the characteristic increase of growth to have taken place in every case, and examples can be found of one-, two-, three-, and four-year-old migrants. Lake Heron differs from Marymere in that there are several small tributary streams flowing in and one fair-sized stream flowing out of it. In the spawning season these are packed with spawning trout. No doubt also a large number of trout spawn in the lake itself. I have selected five fish from the fifteen which appeared to have scales similar in character to the Marymere fish, and calculated the average rate of growth as follows : — Winters . . . . 1 2 3 4 .5 6 ' 7 Inches 5-1 12-2 18-2 20-5 21-7 22-3 23-0 Fig. 7 shows the growth-curve for these, and the broken line shows the growth-curve for the Marymere fish. There is a difference of 1 in. at three years and 0-8 in. at four years old ; elsewhere they agree to within 0-5 in. ^0 i$ \ 16 25 — -"~ ^--j: ;=- — ■ ___^— ^ =-^ 30 ^ — -^"T^^ 20 - ' ^-^_,^^ 18 ,•' // 16 ts /J fi u )j ,^ '/ / fO / / / / s 7 _ S / / ^ / i ^ / 0 / 0 Fig. In dealing with such small samples the agreement is most remarkable, and suggests the probability that these fish were bred in the lake itself or migrated as fry. Trans. N.Z. Inst., Vol. LI. Plate V. CJ . i z .^ SI L'5 rn C1 3 br O n:i o S-i SI 1 — 1 CJ K' o — 1 ^' 50 n o ce ^ o f-t ^ >>H ^ • •^ x 1-^ i Ix ^~ = s 5il 5£' t^ 2 ^ 2 te:S -=■ -^ ^ ^ re t< 3 3 O +j +i 13 o o ?2 25 GoDBY. — GroirtJi of B rou'ii Trout in Canftrhur>i. 55 The average age — 6-93 last winter or 7-93 at next spawning — is again high — higher than Marymere. Lake Alexandrina — This lake contains some very large fish, and the average size is certainly greater than in either of the last two lakes. Unfor- tunately, I have been able to obtain scales from only two fish ; the figures for these are shown in Table IV (C). Lake Coleridge. — This lake was first stocked with brown trout in 1868, and has for many years been noted for the exceptionally large size of its trout. I have been able to obtain scales from three fish only from this lake, but two of them are so remarkable that I have included a photograph of a scale from each fish. Plate VI, fig. 1, shows a scale from a fish of 10| lb. captured about the 5th November, 1917. The length of the fish was not supplied to me, but would probably be about 27i in., and I have made my calculations on this assumjition. The fish seems to have been three years old in the winter of 1917, and shows a most remarkable growth since the last winter. The figures for each year are as follows : — Winters Inches 15f This scale apparently belongs to the Marymere type, and the fish was probably bred in the lake. It is considerably larger than any three-year- old I have ever heard of. The second fish was captured on the 10th March, 1918. A photograph of one of these scales is shown in Plate VI, fig. 2. The fish weighed 17 lb. and measured 34| in. in length. The scales are, I think, the most beautifully marked and at the same time the most interesting in my collection. Surrounding the centre of growth are four winter bands close together, denoting four years of poor growth. These are followed by a year of growth which, so far as I know, is cjuite unique. There is another year of good growth, and then two years of moderate growth. The last winter band is right at the edge of the scale, and it is perhaps open to question whether this represents the winter of 1917 or the beginning of the 1918 winter. The difficulty of reading the scale is increased by the fact that every scale is more or less broken or worn at the edge. The fish was an egg-bound female, and in this abnormal state it is unlikely that she would grow much. On the whole, I think it more probable that the winter band right at the edge of the scale represents the winter 1917, and that there has been practically no growth since then (represented by one or two rings only), and that the fish was going back in condition when caught, as is evidenced by the frayed lateral edges of the scale. On this assumption the figures are as follows : — Winter-s . . 1 2 3 4 5 6 7 8 Inches . . 2i 4 8 lOi 24 30 32i 34i The individual growth-curves for these two fish are shown in fig. 8. It is a fortunate coincidence that in three fish from this lake I should have 56 Transactions. hit on two such striking and extreme examples of different types of growth. The probable weight of the 17 lb. fish each year would be about — 1 Winters . . 1 2 3 4 5 6 7 1 8 1 '' \ \ Weight .. ! loz. 4oz. 4oz. 8oz. 5Jlb. 1 11 lb. ! 14 lb. 1 i 1 lejib. ' 2jy*56 7 a 9 /o / ^^ ly ' .'^'"^ 1 / ,^ . i ^ / 1 / 1 £0 / 1 SO / 1 ' / j ,^ / 1 'f / j / 1 • IS / j / 1 , ,^ / j „ / 1 , / ^ 10 / ^ / ^ / y , / / ^ / y s / y / ^,,-^^ / ^ -^ ;• , / -^ o 0 Fig. 8. Conclusions. 1. The scales of a trout give fairly reliable evidence of age and length attained by the fish each winter. 2. Some scales are difficult to read, and errors may occur mainly in three ways : (a) The first one or two winter bands are often very indistinctly marked ; (6) in very old fish the winter bands may be so crowded together towards the edge of the scale as to be indistinguishable — possibly in some cases the scale may cease growing altogether ; (c) some scales, whilst clearly marked, are at present difficult to read : when this is the case all scales from the same fish present the same peculiarity. 3. A true spawning-mark is not uncommon amongst the large males, and is probably formed by absorption of the scale, especially the outer surface, in formation of the tough skin assumed by the males at spawning- time. In other fish the character of the winter band gives in many cases a tolerably reliable indication of spawning. 4. Under normal conditions trout increase but slowly in length after the third winter. Growth is most rapid in the first two years, and generally the first year shows the best growth of all. 5. Very rarely does a trout growing in this manner attain a large size (say, over 2 lb.). Large trout almost invariably show a break in the growth- curve when a year of rapid growth succeeds slower growth. After the rapid GoDBY. — Growth of Brouni Trout in Canterbury. 57 growth has set in the growth follows the normal curve again, getting less every year. This break or jump is probably caused by migration to more favourable surroundings. 6. Trout which have been stunted by unfavourable conditions for four or even five years, and possibly longer, are still ca])able of rapid growth. 7. Any particular water seems to have' a fairly definite maximum size of fish. In waters where this is large, such as Lake Ellesmere and the back- country lakes, the maximum size will be reached no matter what the age of migration, and the age of migration seems to have little or no effect u])on the size ultimately attained. 8. Lake Ellesmere has a maximum size in the neighbourhood of 23 in., but some fish considerably exceed this. Whether this is due to an mherited tendency to rapid growth or to some specially favourable circumstances I cannot at present say. It is certainly a point worthy of investigation. 9. In Canterbury trout grow much more rapidly in the early stages than in Norway, but the growth slows down earlier. The very large Mjosen trout are mostly very old, and still growing vigorously. The average age of migration is also much higher there than in Lake Ellesmere, for instance. 10. Yearling trout average about 5 in. in Canterbury, as calculated from the scales. From Victoria Lake 112 yearling trout averaged 6 in., but the conditions there are certainly more favourable than the average. In Norway yearling trout average about 2 in. (Dahl). 11. Lake Coleridge seems to favour the most rapid growth of all. The sea is slightly more favourable than Lakes Heron, Marymere, and Ellesmere, which are about the same. 12. Except in very complicated waters, a fair idea of the average growth can be obtained by examining small parcels of ten to twenty fish, provided they aie of fair age and fairly representative. I take this opjjortunity of expressing my thanks to Dr. Chilton for much kindly instruction in microscopy, and to the North Canterbury Acclimatiza- tion Society and many anglers for assistance in collecting scales. The photographs are by Messrs. Leghorne and Colgan, of the Radia Studio, to whom I am much indebted for their infinite pains and trouble to secure the best possible results. References to Literature. (1.) Knut Dahl, The Age and Growth of Salmon and Trout in Norway, as shown by their Scales (translated from the Norwegian by Ian Bailee), Salmon and Trout Asso- ciation, London, 1910. (2.) C. H. Gilbert, Age at Maturity of the Pacific Coast Salmon of the Genus Oncorhynchus, Bulletin U.S. Bureau of Fisheries, vol. 32 (Document No. 767). 1912. (3.) C. HoFFBAUER, Die Altersbestimmung des Karpfen an seiner Schuppe, Allgemeiite Fischerei Zeitunq, Jahrg. 23, pp. 341-43, 1898 ; Jahrg. 25, pp. 135-39, 150-56, 297, Miinchen, 1900. (4.) H. W. Johnston, The Scales of Tay Salmon as indicative of Age, Growth, and Spawning-habit, Fishery Board for Scotland, Ann. Rep., vol. 23, pt. 2, 1904 : vol. 25, pt. 2, 1906 ; vol. 26, pt. 2, 1907. (5.) A. T. Masterman, Rejjort on Investigations upon the Salmon, with Special Reference to Age-determination by Study of Scales, Board of Agriculture and Fisheries, Fishery Investigations, Series 1, Salmon and Fresh-ivater Fisheries. vol. 1, London, 1913 . (6.) H. P. Taylor, The Structure and Growth of the Scales of the Squeteague and the Pigfish as indicative of Life-history, Bulletin U.S. Bureau of Fisheries, vol. 34 (Document No. 823), 1914. 58 Transactions. Table I (A). Thirty -three Trout from Selivyn Stripping, June, 1916. X ^„ "XTrt Sex. Length each Whiter. IjOg No. 1 1 2 3 4 5 6 7 8 In. In. In. In. In. In. In. ] n. All M 3i H 11 18 20 22 A 12 M 5 10 14 22 23* , , A 13 M 6| 13i m 20i 9-> 224 A 15 M H 5| 10 19 21i 23i A 16 M n 7 Hi 15f 20* 22* A17 M 3 6i m 14f 20* 21| 25 A 21 M H 8 14i 16* 19 A 22 M 5 lOi 14| 18| 21i 224 A 23 M 'i 12 17 A 24 M 3i H 12| 16* 201 22 A 25 M 3 6 12| 18^ 21| 23 A 26 M 6i 9| 14i 17| 21 , . A 27 M 5 8i 10| 15 19* 20i 21 : 224 A 30 M 6i 12 18 20 20f 22 A 31 • M 6 ui 18i 20 , , A 32 M 6 lOf 18* 23 25 , , A 33 M H m 17 20 21f 234 A 34 M 4i u 91 12 16 . . A 35 M 4 151 18 19 20* 214 22 A 36 M 6 14 18J 194 21i 224 A 37 M H H 13* 17 19f 22 23 A 38 M 3* «i 12 184 194 , , A 39 M 3| H 18i , , , , . , A 40 M 5f 10 18i 23 , , A 41 M 5i 12| m 20i 234 25 A 42 M H 7 12J 15i 171 21 A 43 M H 7i 10* 15i 174 A44 M 6i 12 18* 21i 23 , , A 45 M 4i lOi 13 m 21i A 46 M 4| m m . , A 47 M 6 m 18* m . , A 48 M 3i H 1-4 m 19 194 20 A 49 M 4| 7 11* m Aver ages • 4-7 9-7 14-7 lS-3 20-7 22-2 22-2 2 2-5 s Average age Average length . . Average length of 100 males marked in 1915 5-4 21-3 20-8 GoDBY. — Gruirtli of Brown Trout in Canterbvry. 59 Table I (B). 140 Trout from Selwijn Stripping, 17th June, 1917. Log No. a „ Length each Winter. Sex. 1 • > 3 4 5 6 7 8 9 10 11 In. In. In. In. In. In. In. In. In. In. In. A 50 . F n 13 15 17i 204 21 214 A 51 . F 4 n 124 184 20 , . 1 . . A 52 . F 5i 8i 134 164 18|- 21| . . * A 53 . F 4i 7| 17 204 A 54 . F 4* n 13i 184 21 , . A 55 F H ~'i 114 15.^. 171 19 204 A 5(5 . F 6i 12 184 204 21| 23 A 57 F 4i n 12 174 20 , 214 23 A 58 . F 4 74 n 13 14J 17 19 264 214 . A 59 . F H 7 11 13f 16f 184 194 AGO . F 6f 124 184 A 61 . F 6f lOi 14 184 21 A 62 . F H 8i- 12i 14J 174 194 20i A 63 . F 4i- H 134 16 17-1 19 A 64 . F 5^ 10 134 16 18 194 A 65 . F U 11 144 16| 18 19 19f 264 A 66 . F 5f 12 18 . , , ^ A 67 F 5f 10 144 18 194 204 21 A 68 . F 5| 104 14i 164 184 204 , , A 69 . F 7 10* 131 17 181 204 , , A 70 . F 7 14t 174- 184 204 • A 71 . F 4i 9 124 16" 184 204 A 72 . F 3J n Vlh 19 * • B 1 . M 5 8i 17 224 27 B 2 . F H 124 184 . . . , B 3 . F U 12 144 16 174 18 181 194 264 B 4 . F 5 8 104 144 164 194 204 21 B 6 . F 4 74 104 16i 20 23 , , B 7 . F 4i 94 164 18 19 20 261 214 22 B 8 . F 4 9 144 17 194 204 224 B 9 . F 7 13 16 184 BIO . F 6i 9i 13i 174 . , , , , , BU . F of 134 19 B12 . F 44 lOi 14i 174 194 B13 . F 44 8 14 16 184 ■ih B14 . F 5 14 194 B 15 . F 3 7 12i 164 184 B 16 . F 6 10 174 19 21 • . B 17 . F n I3i 18 . B 18 . F 4f 8| 15 174 i84 21 B19 . F 4 84 12 174 B20 . F 6i 114 151 18f 20 2i4 , , B21 . F 5 9 13 164 184 20 B23 . F 7 I3i 161 18i 20 214 22 . 224 B24 . F 5 lOi 18 194 21 B 25 . F 6i lOf 15 18 20 2i4 * B26 . F Vi- 111 15 17f 191 21 , , B27 . F et 124 154 18 194 21 . B28 . F 6 91 12 14t 184 20 224 B29 . F 4 n 134 19 B 30 . F oh 9 114 14 164 264 B31 . F 41 94 124 144 174 19 60 Transactions. Table I (B)- — continued 140 Trout from Selwyn Stripping, 17th June, 1917 — continued. Log No. Sex. Length each Winter. 9 10 11 B32 B33 B34 B35 B36 B37 B38 B40 B41 B42 B43 B44 B45 B46 B47 B48 B49 B50 B51 Bo2 B53 B54 B55 B56 B57 Bo8 B59 B60 B61 B62 B63 B64 B65 B66 B67 B68 B69 B70 B71 B72 B73 B74 B75 B76 B77 B78 B79 B80 B81 B82 B84 B85 B86 In. In. In. In. F 7 Hi 14i 17* F 5i 10|- 16 19| F 4 m 18i . . F 6f m 16i 17f F 5i -i 13i 19 F n 12i 16i 18* F 6| 13i 18i F H -i 13i 17* F 7 11-1 14f 18 F 8i 11 14* 17 F 5i n 8| 14f F H 11 15i 17* F U Hi 14| 17 F 3i 7 14* 17 F 3f 6f 9i 12* F 5^ Hi 17 20 F 3f H Hi 15i F 6i 12 16f 181 F 4 7i 13 18i F 4i 11 17 18f F ^ lOf 15* 17f F 3i 6 9i 121 F 5* 8i 11* 151 F 5 8i 13i 18* F H 71 Hi 15 F 5i 12 16* 19* F H 8i 131 16 F 5 12i 17 19 F 6i 8i 12i 17 F 31 6i 9 16i F 41 n 10| 141 F 5i H 14* 18i F 4i n 12i 18 F 5* 81 11* 15* F 4i 8| 13| 16 F 51 111 131- 16* F 3i 9 13 17 F 4| 8f 11* 18 F 4i 9 13* 15* F 4f 81- 13i 17i F 4| 8i 14 19 F 3i 5i 9 12| F 6i loi 18 19* F 4i n 12 18* F 5 8i 11 13 F 4i 8i 131 18* F 3i 5h 9i 13i F 5i m 14f 19i F 5i 8i 12i 17 F 3i 61- n 13* F Si- 8i 13i 16* F Si 11 m 19 F 5i 9i iif 15| In. 20 16* 20 18i 18* 19 19* 21 20* 18* 16| 19* 18 20* 18 13J 19i 20* 20* 19i 17* 18* 20* 17i loi 21 16 21 20* 16i 18i In. 20 21^ 21 18 20* 21 19 21 20* 20 20i 19 21i 15i 17 18 21* 18* 19i In. 21 21 20 i9; 20 22* 20* 20* 23 19 19 20 21 2i In 22 21i 23 In 23 20 In 21 In. GoDBY. — Growth of Broiim Trout in Canterhiirn. 61 Table I (B) — continued. 140 Trout from Selwyn Stripping, 17th June, 1917 — continued. Log No. Sex. Length each Winter. 1 2 3 4 5 6 7 8 1 9 1 10 11 In. In. In. In. In. In. In. In In. In. In . B 87 .. F 3i 54 104 14i 16^ 18i 194 , B 88 .. F 3| 9f 15i 17| 19i 21i 22i 234 B 89(a) F 6i 9 llf 144 17 184 20 , B 89(6) F 5i 8i 144 19i 21f 221 234 ■ , B 90 . F 4 6f 13i 17 17J 194 20 204 B 91 . F 4| 7 10 14i 16 18 204 ■ , B 92 . F 6 13 16 181 214 B 93 . F 4 74 114 13| 15* 17i 18| i 194 20 B 94 . F 54 n 14| 17 19i 20 21i , 22 B 95 . F 4 71- 12| 174 194 21 224 I • B 96 . F 3i 6 13f 20 . , . B 97 . F ^ 64 13 154 17i 18i 20 2 ii B 98 . F 5 8f Hi 134 154 184 20* 224 B 99 . F 4 10 12i 14| 17i 184 194 • BlOO . F 5i 84 lOf 13 16 184 191 2 1 1 BlOl . F 4 8 114 14 15| 171 18 1 9 2i B102 . F 8 12i 15| 184 • . B103 . F 4 7i Hi 134 15 B104 . F 4i 144 19 214 . , 4 • • B105 . F 5 84 14| 17i 19i 214 < . B106 . F 4 6f 11 14 16| 18 194 • B107 . F 4i U 14| 184 20i 224 B108 . F 4 7| Hi 13| 164 184 204 • B109 . F 4* 74 11 15 181 194 21 BllO . 4* 8| 14 194 , ^ Bill . F 5 8f 12-1: 18 . . B112 . F 4 7i 94 12 1.5f 18 . • B113 . F 5i 11 18 , , B114 . F 5i 84 13i 194 . . . B115 . F 5* 10| 18 B116 . F H 8 11 14 174 20 204 -' 2 B117 . F 6f 12| 16 18 , , B118 . F 5i 114 15i 17f 20i 22 . . B119 . F 24 5 6 84 Hi 14 15| 1 8-1 194 20| 22 B120 . F 4 8 15 17 184 201 224 2 3i 244 Ave ra ges .5-1 9-3 13-8 16-9 18-6 19-8 20-6 21 2 21-5 2M 22-0 1st twenty 2iid twenty 3rd twenty 4th twenty 5th twenty f)th twenty 7 th twenty Averages for each Group of Twenty. 5-3 9-4 14-0 17-0 18-8 20-0 20-6 20-5 21-5 5-2 10-3 15-3 18-2 19-6 20-3 20-5 20-7 21-2 5-8 10-6 14-8 17-6 19-3 20-7 21-7 22-5 , , , , 5-2 9-5 13-7 16-9 18-8 20-0 20-7 22-1 23-0 4-7 8-4 12-5 16-7 18-7 19-2 20-6 20-6 21-2 21-5 4-5 8-4 12-6 16-1 18-0 19-4 20-6 21-5 20-0 4-7 9-0 13-5 16-2 17-1 19-2 19-7 20-7 21-7 20-7 22-0 Average age Average length. 5-9 20-4 62 Transactions. Table I (C). Twenty -nine Trout (Males) from Selwyn Stripping, 16th June, 1918. Average age Log. No. Length each Winter. 1 2 3 4 5 6 7 In. In. In. In. In. In. In. B 235 . 3* 6 131 20 . , B237 . 4 14* 19i 22* 241 B239 . 3J 6 13* 18 20* 22 22* B240 . 5 13 17 19i 21f 23 B241 . 3i 7 15 . , , , B 242 . 4i 8i 13 201 21* . , B243 . 8f 14f 17f 20 22f 24 B244 . H 7 14 20* 22 23 B247 . di 9| 13* 21 23* . , B248 . 3f 8i 141 201 21* 24 B 250 . H lU 20* B2ol . 6 14 19* 2li 22* B252 . 6i 15 22 26 B2o4 . 6| 13* 18* 21* 23* B 255 . 7f 14| 20^: 22 ■ , . B256 . 7i 15* 21* , , B 257 . H 6l 8 H 17* 24' B259 . 7 131- 21 24 B260 . 4 8 12* 21 23 B 2r3l . ii & 17 . , , , B 262 . H m 20 23f 24* B269 . 5i Hi 15 21 23 25 26 B270 . 6^ 13i 21i 2.J B271 . 6f 12f m 23i 26* B276 . 4i 9i 17 ■2H 231 24" C 3 . 6 15* C 5 . 5i 8i 16* 19* . , C 8 . 4i 7i 13* 18i 20f 22 (' 13 . H 15i 20* 23* 25 A^ ^erages . • 5-5 10-9 16-8 20-9 22-5 23-5 24-2 Average length Average lengtli of sixty-six males marked in 1918 4-8 22-5 22-6 GoDBY. — (yroirth of Broirti Trout in Cfintfrhxrii. 63 Table I (D). Thirty-six Trout (Females) from Selwijn Stripping, 16th June, 1918. Length each \\ Inter. Log Xo. 1 2 :i 4 5 6 7 8 9 In. In. In. In. in. In. In. In. In. B236 4 6f 14| 17i 19J 21 21* B238 8 13i 161 18* 20 2 If 23 24 25 B246 4| n 13i 181 21 22* , , B249 7 12-i \Sh 19* 20f 21| 22i 24| 251 B253 -ti 7i m 14* 16f 19 211 22* B263 7i 13" m 17* 20 21 B264 H 14 16f 191 211- 22* , , B26o •H 14 i5i 171 19 20* 21* B266 7f 13i 18 B267 ••i lOi 1-ti 21 24 , , B268 4 Ih Hi 16i 171 19 20 B272 4 8i loi 20* B273 5* 10 13* IS* 201 23 24 251 26 B274 •u 7| 14i 17i 19i 21* 22f B275 4 13i 19* 20* 22 23 B277 6i I2i 16* 18f 20* , , B278 3| 7 10 12f 15f 18* 19i 21| 22* B279 ->f 111 16 171 19 20i 21* B280 •5f 13 19 B281 3i 6 lU i7* 26i 21 22i 23 B282 8i 14i 19i 21 B283 6i lU 16 18i 19* 20i- 2i B284 41 7i 13* 19i 21 , ^ B285 U 6i loi 171 m 21 22 B286 81 (ii n l-tf m 20i 21* B287 7 12* 15 17* 20* 22 B288 5i 9i 13* 18f 20 . , , , , , C 1 4 5! 8* 15 17 18* 21 22* C 2 7 Hi 14i 17 i8i 20* ■in C 4 5i 12! 16 18i 20 21 C 6 7i 14i 21 23 C 7 -t* 71 13i 161 19 20* C 9 4 13i 19* _ C 10 6i 13-1- \n ig C 11 5 9 13* 17J 20* C 12 3| 51 lOi 14f m 19| 21 22 Aver ages 0-4 10-3 14-9 17-9 19-6 20-8 21-6 23-2 24-7 Average age Average length . . Average length of 156 females marked in 1918 6-2 21-7 21-5 64 Transactions. Table I (E). Thirteen Trout caugM with Rod and Line, Lake Ellesmere, 1917-18. Date. Log Xo. Weight. Length. Sex. Length each Winter. 1 2 , 1 . 0 6 7 -- lb. In. In. In. In. In. In. In. In 20/10/17 . B132 11 28 M 5f m 13i 184 'i 244 26| 21/10/17 . B133 6f 25 Fl 4* 84 13f 164 19 214 24| 27/10/17 . B136 5i 23 F 4* H 14i 17 19 214 17/11/17 . B147 8J 28 M 3f 10 16i 224 27i 17/11/17 . B150 H 22 M 5* H lU 14|- 16f 211 17/11/17 . Biol H 22 M H m 13 15i 20 17/11/17 . B152 24 m F H 84 llf 15 . . . , 9/12/17 . B159 3i 21 F 5 74 134 151 m 20 8/1/18 . B185 U 25 . . 4i 94 16 191 214 241 6/1/18 . B198 n 24 F 6* 12| 22 . . . . . , 9/3/18 . B213 7 24 F H 9 14f 194 22i 9/3/18 . B214 7 25i F 6f m 18f 22-1- 9/3/18 . B216 4 19| M 5 n Hi 16| Averages 5-1 9-7 14-6 17-9 20-8 22-2 25-7 Table I (F). Five Large Trout from Lake Ellesmere. Log KTo. Length each Winter. Date. M M> W a 0) X 1 2 3 4 5 6 , 7 8 9 is- ^^ TH lb. In. In. In. In. In. In. 1 In. In. In. In. 28/12/16.. A 1 134 284 F 6 9i 214 254 274 . . • . . . -/6/15.. A 18 iH 29 F 5* 8* 13 17 214 234 251 264 27^ 20/10/17.. B132 11 28 M 51 10* 13i 184 22f 244 26i 17/11/17.. B147 8| 28 M 3| 10 16i 224 271 10/5/18.. B232 134 33 M n 13 17 211 274 31 Averages . . 5-8 10-2 16-2 20-9 25-3 26-5 26-0 26-5 27-5 GoDBT. — (Jrowth of Brown Trout in Canterbury. 65 Date. 1/10/17 1/10/17 4/10/17 i/io/n 26/10/17 26/11/17 23/12/17 9/10/17 9/10/17 9/10/17 8/12/17 8/12/17 8/12/17 8/12/17 30/12/17 30/12/17 8/4/18 24/2/18 24/2/18 24/2/18 7/10/17 7/10/17 13/10/17 14/10/17 28/10/17 28/10/17 28/10/17 28/10/17 9/11/17 .. 10/11/17 .. 9/11/17 .. 10/11/17 .. 9/11/17 .. 9/11/17 .. 9/11/17 .. Averages Table II. Rain Rivers. Log Xo. B 127 B128 B129 B161 B103 B 165 B169 B173 B 174 B231 B208 B209 B210 B125 B 126 B130 B131 B137 B 138 B 139 B 140 B162 B 164 B 166 B 167 B170 B172 B 168 Weight. I Length. Sex. Length each Winter. A . Cam. lb. In. In. In. In. In. In. In. B121 2i 18 4^ 8f m 14f 16i 18 B122 i 12 5 10| . . . . B123 15f 6* m iH . . B124 . , 15i H m 14 ■ . B 134-5 1 14| 4 8 12 i4i . . B153 1* 15-2 4 n 10|- 13* 14i B 160 If 16i F 5i n 13^ 15 B. North Branch, Waimakariri 8* , , 6i . , , . . . f 14 . , 4^ 8 Hi 13* i Hi . . U- 9i Hi H 14i F 4 H m H 14f M H Hi 13i f 12 , . 4i 10 u 15* M 4|- n 13i li 15 4 n 13i h Hi 5i m H 18i M 5* H 12f C. Slyx. n 15 3| 9 1 13 .. 3* 6 i- lOJ .. H H 131 9J E. Opihi 10* 10 13* 10 11 13^ 11 uiirJ Tengawai •J 4 4 3i 4f 5i 4i u 7 6 8i 9i 7i 4-6 9-0 9* 11* 12-0 11 13 13-7 D. Selwyn No. 2 2 18 M 6i 10* 13f 16 16i 1 n i IH . , 5i 10 12| 12f , . ^ 7i 10^ m . . li m F 5 9* 13i 141 15* 1 14 . , 3i 6i 12^ 13| li 15i 9i M 4 3f f 13 14 15 f 13i 5* 12 121 14- 17-7 A verages for each River. A. Cam 5-0 10-0 130 14-4 B. North Branch, Waimakariri 4-8 9-0 12-5 13-5 C. Styx 3-6 7-2 11-5 12-9 D. Selwyn No. 2 4-7 9-0 12-7 141 E. Opihi and Tengawai . . 4-2 7-5 10-0 12-2 15-5 I 18-0 .. I .. 12-2 15-7 17-5 12-7 3 — Trans. 66 Transactions. Uatc. Table III. Svoiv Rivers. Log No. .SP 'S 6C Length each Winter. 23/1/18. 23/1/18. 7/3/18. 7/3/18. A. A Men. lb. In. In. In. In. In. In. In. In. In. B19o H 24* U llf 16i 20i 22^ .. 1 B197 3| 201 F H 11 161 , . , , B212 3 18* M 6 10 14 16 J B215 4i 204 . . 5 8 14f 171 20 In. B. Waimakariri. 3/12/17. 3/12/17. 30/11/17. 23/1/18. 28/1/18. 2/2/18. B154 H 17 M 4 B155 12 3* B156 If 16 F 3f B194 4^ 2U M H B196 2* 18 M 5h B202 9i "4 171 F 5* B217 34 20 4f Hi 10 10 12 134 14f . . 1 . . 8i 104 , , . . . • 1 . • lOf 14 144 161 18| 20| 16 131 17 . . 14i 18 . . 1 C RaJcaia. 10/11/17. 12/1/18. 11/1/18. 20/1/18. 3/2/i8. 10/2/i8. Averages . B 144 B190 B192 B193 B 199 B200 B203 B204 . , 234 M 64 25 F 5 244 M 1 14 F 44 21 F 7 28 F 44 21 F 3 19 M 54 4i 5i 5 74 54 4 4-7 134 9| 10| llf 114 10 8| 84 18 14| 18 15 m 9-7 14-3 114 22f 23i 164 i 18| 24 18 25f 17-1 19-7 154 21-1 195 21-5 ■?3 "4 22 A. B. C. Ashley Waimakariri Rakaia Averages for each River. 5-3 10-2 15-4 18-1 21-4 , , 4-6 8-7 12-8 14-9 16-7 20-7 , , , , 5-1 10-2 15-3 18-8 20-2 21-1 19-5 21-5 22-7 GoDBY. — (rrowfh of Broiru Trout in Canterbury. Table IV. Back-country Lakes. 67 Date. Log No. J3 -6 a Length each Winter. 10 A. Marymere. 23/12/17 24/12/17 24/12/17 23/12/17 27/12/17 27/12/17 26/12/17 26/12/17 24/12/17 25/12/17 lb. In. In. In. In. B175 4* 23 M 3* 10 15^ B176 6 24 F 6 12 15f B 178 H 2U F 6 15i 19 B179 U- 26 M 6 12^ 16 B180 6 26 M of 13i 18i B 181 7 27 F 4f 12 16f B 182 5 22 M 4* 13 191 B183 4* 20^ F 4* 12 18 B188 5* 24 F 6 12* 15* B189 7 26 F 6| 131 17f In. 17^ 17f 20 21| 20| 20 20J In. 19* 20i 221 23| 221 2i 21^ In. 20f ''* 23* 241 24 22 22f In. 21| 221 24* 25i 231 23* In. 221 23 25* 26i 24i In. 251 In 2/11/17 2/11/17 1/11/17 8/11/17 24/11/17 31/3/18 31/3/18 31/3/18 31/3/18 31/3/18 31/3/18 31/3/18 31/3/18 31/3/18 31/3/18 B. Lake Heron. B142 6 24* .. 2* 7 10* B143 5 21* 3f 6f 9| B 145 8 26 ivi 4f 9 18 B 146 6 24 4 u llf B158 8 26* M 4* 7* 10* B221 5 •2l\ M 4* 8* 16 B222 5 22| M 5* 10* 17* B223 5* 22| M H 12f 19* B224 6 23* F 5 11 19 B225 61 24 M 5 m 16 B226 4 993 F 3* 6f 8f B227 6 22^ F 5^ H 14 B228 5 21* F 4 6* 11* B229 4* 19f F 4 6^ 13* B230 7 24| M 5 14* 191 17 21 23i 241 . , , , 11* 17 19 20* 2U 21* 22| 23* 24* 251 25f 17f 20* 21 22 22f 231 23 17* 20i 23* 24f 26 201 , , . , , , 20 21^ 221 , , , , 20f 21| . , , , , , 20* 21| 22^ , , 19^ 20* 22 23 15 18 19* 20| 2i| m 18 21 22^ . , , , m 181 19f 20f m m m 19 221 231 . . 10/2/18 10/2/18 B205 B206 f;3 10 ooi 281 C. Lake Alexandrina. M ] 6 I 11* 16* F 51^1 11 17 ; 41 221 26 27^ r- 5/11/17 10/3/18 3/6/18 D. Lake Coleridge. B141* 10* 27* F 7 15| 234 B218 17 34* F 2* 4 I 8 B234 20 33* F 3* 7 i 12^:1 19* 24 26* 30 31* 34i r^p-p ' Averages A. Lake Marymere 5-4 12-6 17-2 19-7 21-5 22-7 23-4 24-2 24-4 B. Lake Heron . . 4-4 9-0 14-4 18-2 20-4 21-5 22-6 230 23-7 23-7 ., "natives" 51 12-21 18-2 20-5 21-7 22-3 23-0 j , , ,, " migrants " 4-1 7-4 12-4 17-0 19-7 21-2 22-5 23-0 23-7 1 23-7 * The length of B 141 (Lake Coleridge) was estimated from the vveiglit. Marymere — Average age, calculated as at last winter : 6-40 ycar.s. Lake Heron — Average age, calculated as at last winter : 6-93 years. 3* 68 Tranmctions. Art. VII. — Description of a New Species of the Family Cerithiidae. By Henry Suter. Communicated by R. Speight. [Read before the Philosophical Institute of Canterbury, ISth September, 1918 ; received by Editor, 25th September, 19 IS ; issued separately, 14th May, 1919.] Fastigiella australis n. sp. Shell elongate-conical, gradate, many-whorled, with slightly nodulous cinguli ; aperture oval-quadrangular ; columella with a distinct fold pro- duced by the entering of the carina of the fasciole. Sculpture : The post- embryomic whorls have a prominent convex and faintly nodulous spiral band below the suture ; a similar but narrower band above the lower suture, and below it a fine thread margining the suture. The paratype, which is smaller, shows only the upper band and a distinct thread above the suture below, (^n the lower whorls the thread margining the suture is lost ; strong convex and distant growth- lines turn up which are produced into nodules on the upper and lower cinguli, but the speci- mens before me, no doubt considerably worn, show only traces of these characters. The body-whorl is distinctly angled and bears two cinguli upon the angle. The base of the paratype shows traces of spiral striation. Spire high, distinctly gradate, angle about 20°. Protoconch lost. Whorls 8 on the im- perfect holotype, flat or somewhat concave between the cinguli, the body-whorl angled. Suture deep, canaliculate in the paratype. Aperture ovate, but slightly quadrangular, not channelled above ; most likely with a very short and notched canal, but the whole of the mouth is too much damaged in both specimens to be quite certain. Outer lip straight, curved and indistinctly angled towards the base. Columella a little excavated above, bearing on its lower part a fold which evidently extends as a carina upon the fasciole, but the latter is almost completely broken off. Inner lip spreading somewhat over the base, more apparent on the paratype. Height, 22 mm. ; diameter, 8 mm. (imperfect holotype). Holotype and one paratype in the Canterbury Museum, Christchurch. Zoc— Holotype from the upper horizon, Whitewater Creek, and the paratype from the upper horizon, Struthiolaria bed, Porter River, Trelissick Basin ; both collected by Mr. R. Speight, Curator of the Canterbury Museum. Remarks. — The genotype is Fastigiella carinata Reeve, a living species from the Antilles, and our species differs from it chiefly in the aperture not being channelled above. The umbilicus of the type I take to be simply Fastigiella australis Suter. SuTER. — A New Species of the Family Cerithiidae. 69 a deep impression inside the fasciole ; Cossmann does not mention an umbilicus in the diagnosis of the genus. Besides the Recent genotype, about half a dozen Tertiary species are known, the genus being evidently of rare occurrence. F. cmstralis is, as far as I know, the first species recorded from the Southern Hemisphere. The Cerithiidae are but scantily represented in the New Zealand Tertiary. At the present time the following six species are on record : Cerithium hectori Harris, Besanconia huttoni (Cossm.), Fastigiella australis Sut., Cerithidea hicarinata (Gray), G. tricarinata Hutt., and Balillaria pomahakensis Harris. Art. VIII. — The Structure of Amphibola crenata Martyn.'^ By Winifred Cheyne Farnie, M.A., Assistant in the Biology Depart- ment, University of Otago. Communicated by Professor Benham. [Read before the Otago Institute, 9th October, 1917 ; received by Editor, 17th December, 1918 ; issued separateh/, 14th Ma;/, 1919.] Introduction. The shell of Amphibola was first brought to the notice of European naturalists by being collected during Cook's voyage to New Zealand in 1769, but the earliest account of the anatomy of Amphibola we owe to Quoy and Gaimard in 1832. The only other accounts we have are those of Captain Hutton in 1879 and 1882, and of Bouvier in 1892. f Quoy and Gaimard (1832) described specimens collected in New Zea- land during the expedition of the " Astrolabe." They ascertained that it was a true pulmonate, and that it was hermaphrodite. They give excellent figures of the shell and operculum, but only one of the internal anatomy, and that is lacking considerably in detail ; while their account of the anatomy is inaccurate in several points, and not sufficiently detailed. Captain Hutton (1879) noted the two small triangular tentacles, and described the kidney and alimentary canal in greater detail than Quoy and Gaimard, though his description of the intestine is not quite correct. He also figured and described the nervous system and reproductive organs. In 1882 he published some further notes, wherein he corrects his former account of the radula and traces what he took for the '' oviduct " from the hermaphrodite duct. Further mention of Hutton's work will be made throughout my account. For a systematic diagnosis of the species reference should be made to Suter's Manual of New Zealand Mollusca (1913) and Atlas of Plates (1915). * This paper fonned the basis of a thesis for Honours in Zoology at the University of New Zealand, 1916. f I have been unable to consult tliis memoir. 70 Transactions. Although in the original thesis submitted to the University of New Zealand the histological structure of the various organs was discussed and illustrated, I have thought it advisable to omit these matters in the present paper. I wish here to express my indebtedness to Professor Benham for his valuable suggestions and great help in preparing this paper for publication. Habits. Am-phihola crenata is a basommatophorous pulnionate gasteropod found living on mud-flats in sheltered bays, both in brackish and in salt water. It belongs to a series of pulmonates sometimes termed " gehydrophilous " (Cook, 1895, p. 18), in which, while the gill has been replaced by a '' lung," the animal has not become truly an inhabitant of fresh water. Amphibola and some other genera, such as Gadinia and Siphonaria, are '' intermediate between essentially fresh-water and essentially marine species." The larger specimens of Amphibola are found cjuite close to the sea, the smaller ones farther up the mud-flat. They occur in enormous num- bers on all the flats around the Otago Harbour, and, indeed, all along the coast of New Zealand. They are, of course, covered during high tide, but are exposed to view at low tide, so that the greater part of their life is passed out of water. Nevertheless, sufficient water is retained in the mantle-chamber to keep the tissues moist. These animals are exceedingly sluggish. When they are in their natural surroundings one has to watch them very closely to see whether they are moving or not ; but if they are placed in a little sea- water in a dish their method of locomotion is readily studied. When examined on the shore the only evidences of movement are the slow twirling of the shell as it is being drawn up to cover the slightly extended head and foot, the latter of which is concealed in the mud, and the furrow traced out on its path. The most striking feature of this movement is the very small part of the foot that is exposed at any one time. Its method of locomotion is as follows : A small portion of the anterior part of the foot is protruded, and this acts as a temporary anchor. The shell is then drawn up to cover the exposed part, and as it is twisted from left to right during the process it leaves a small part of the foot exposed on the left side and behind. The animal then glides slowlv forward for a space without Fig. 1. — AmjjhiOola crenata from below (natural size), as seen creeping up the side of a glass vessel of fresh water and thus exposing the whole of the foot. The two lappets of the heatl pro- ject only slightly in front of it. /, foot ; h, head ; m, mouth ; s, shell. a space twisting the shell at all. The above process is repeated, the movement of the shell sometimes being from right to left . The shell is carried at an angle to the surface on which the animal is walking, the right side of the shell being raised a little from the mud, while the left side almost touches it. The animal is very sensitive, retracting into the shell at the slightest touch or at any disturbance of the water. Although air-breathing, Amphibola is able to live a considerable time immersed in water, either fresh or salt. If kej)t in a glass of fresh water the cover of wliich is sealed up it will live for a week ; if completely Fah]S'ik. — The Structure of Amphibola crenata Martyn. 71 immersed in fresh water but not so sealed up it will live for a fortnight ; if completely immersed in sea-water it will live a month ; but if left with- out any water at all it does not live more than a day. Even when the tide is low there is always a certain amount of water left in the mud, so that these animals are not, in their native habitat, left absolutely dry. External Features. As Suter gives a good technical descrij)tion and figure of the shell it is unnecessary to deal with it here. The animal is of small size and of a beautiful rich black colour. The head is but slightly marked off from the foot, and is relatively of great breadth (fig. 2). Its anterior region is rather deeply excavated in the middle line so as to form a pair of lappets, one on each side of the mouth. Some distance from these are situated the pair of small, flat, triangular tentacles, which in the majority are so deeply pigmented that the minute eye is not readily seen, but in paler specimens the eye is recognized as an extremely small black dot of darker pig- ment close to the tip of the tentacle. Quoy and Gaimard, though mentioning the eyes, failed to note the tentacles. Hutton (1879), however, de- scribes the latter, but states that the eye is at the base. This error is repeated, naturally, in Suter's Manual, but any one who examines the creature with sufficient care will be able to confirm my statement."^ The foot is short, and almost circular in outline, as seen from below (fig. 1). In preserved spe- cimens it is very much shrunken, but if examined when the animal is walking it will be seen that the foot is capable of being expanded until a narrow margin is visible beneath the shell all the way round except on the right side. The foot is separated from the head by a slight furrow ; there is no distinction into pro-, meso-, and meta- podium, nor have I found any trace of a creeping-sole is cream-coloured Fig. 2. — Dorsal view, of the animal removed from the shell { X 2). The foot is bent upon itself so that the ventral surface of its posterior region is seen in front of the head. Some of the interior organs are seen by transparency, e, eye ; cj, groove into which anus opens ; gp, genital pore ; gz, gizzai'd ; int. intestine ; ipl. inferior jiallial lobe ; k, kichiej^ ; m, mouth ; mc, collar ; pa, pulmonary aperture ; rl, right lappet of head ; t, tentacle ; vf, ventral surface of foot. pedal gland. The anterior part of the the posterior part greyish-blue. * It is not surprising that the tentacles were overlooked by the earlier zoologists, if they had only preserved specimens at their disposal, for when the head is contracted they are difficult to distinguish from wrinklings of the body-wall. As to the eye, in ordinary specimens they, too, are indistinguishable in such material : it is only in fresh specimens and in those in whicli the pigmentation at the tip of the tentacles is less than usual that they can be seen. [W. B. B.] 72 Traiisactions. Attached to the dorsal surface of the hind end of the foot is the oper- culum, closely underlying the shell so as to be visible only from the side. When the animal is completely retracted it fits close against the entrance to the spiral portion of the shell, and is firmly held there by muscles. This characteristic prosobranchiate structure is found in this genus only amongst the Pulmonata. The thickened edge of the mantle, which, of course, is fused with the neck, and which is usually called the " collar" (fig. 2, mc), is light in colour, and is very muscular. It does not project beyond the shell during loco- motion, but if the animal is allowed to remain in fresh water the head becomes expanded and the mantle-edge appears under the outer lip of the shell. The upper lip of the pulmonary aperture is then seen fitting into the sinus of the shell. The margin of the pulmonary aperture is not a simple circular aperture as in Helix, but the lower lip is produced outwards into an " inferior pallial lobe " {ipl) such as occurs in Chilma according to Lang (1900). This lobe is deeply grooved, the groove being triangular in shape, with the apex directed backwards towards the pallial chamber (fig. 2, g). The anus is situated at the apex of this groove. Hutton (1879) describes and figures the anus as being to the right of the pulmonary aperture, and both Hutton and Quov and Gaimard draw the triangular furrow mentioned above as if it were part of the rectum. The anus is really posterior to the pulmonary aperture, although it is capable of being carried beyond it by the extension of the inferior pallial lobe. When the faeces are passed to the exterior the lips of the triangular groove probably close together, so that it is temporarily converted into a tube. This prevents any faeces entering the mantle-cavity. The inferior pallial lobe is also capable of closing against the upper lip of the pulmonary aperture. Internal Anatomy. Organs of the Pallial Complex. (Fig. 3.) The most conspicuous organ on the roof of the mantle-chamber is the kidney, which presents several remarkable features. It is pure-white in colour, and occupies the middle region of the mantle, across which it extends obliquelv for about two-thirds of its breadth : somewhat flask- shaped in outline, its apex is situated a short distance from the pulmonary aperture, its broader base close to the left side of the roof of the mantle- cavity. Running along its ventral surface is a narrow band of muscle {mu) which arises from the middle of the hinder edge of the columella-muscle, which is not shown in the figure. The portions of the kidney on either side of this band are of unequal sizes. The excretory aperture is a conspicuous longitudinal slit on a papilla at its anterior end (ex), which projects freely from the mantle itself. The wall of the kidney is thick, and internally bears numerous filiform papillae which almost fill its cavity. The excretory products can be seen by teasing up a portion and examining it in the fresh state : they appear as clear spherical vesicles of dift'erent sizes, each of which has a very thin envelope of a protoplasmic nature, surrounding a drop of hyaline, non-granular fluid. In the centre of this are several round concretions of a brownish colour. Since the cells of the kidney are not ciliated, they will be unable to aid in the removal of excretory products. Probably the muscle-band which Farnie.— 77jf Structure of Ampliibola crenata Marfj/u. 73 runs along the dorsal surface of the kidney serves this purpose, by com- pressing the flow and so driving the stuff forwards to the pore. Lying on the roof of the mantle-cavity, close to the anterior end of the kidney, and extending a short distance underneath it, is an oval mass of white rounded particles covered by a thin pigmented membrane (hy). It is situated in a curious depression which extends from the anterior end of Fig. 3. — General dissection ( X 2). The mantle, which has been cut along the collar and along the right side, has been turned to the animal's left, exposing the pallial comi^lex. The head and neck have been opened to disclose the alimentary tract and part of the genital system. The rectal sinus has been severed at the point se, where it passes on to the roof of the mantle -chamber. ag, albumen-gland ; as, anterior sinus ; c, crop ; re, cut edge of collar ; cd, common genital duct ; ce, cut edge of mantle ; d, depression in front of renal pove ; dgl, digestive gland ; div, diverticulum of oesophagus ; ex, excretory pore ; g, groove into which anus opens ; gp, genital pore ; gz, gizzard ; hgl, hermaplirodite gland ; hi/, hyj^obrancliial gland ; irs, inferior rectal sinus ; int, intestine ; k, kidney ; I, lung ; Id, duct of digestive gland ; m, mouth ; mc, collar ; mv, muscle-band on kidney ; 06', osphradium ; pa, pulmonary aperture ; pe, penis ; ])r, prostate ; pv, pul- monary vein ; r, rectum ; se, cut end of rectal sinus ; sg, salivar,y gland ; srs, superior rectal sinus ; st, stomach ; I, tentacle. the kidney to the edge of the mantle above the pulmonary aperture. When these particles are disturbed with a brush they give off a bluish fluorescent foam, which quickly re-forms as often as it is brushed away. When examined under the microscope the mass is seen to be made up of rounded particles of different sizes, which contain crowds of small granules. Though white by reflected light, the particles are brown by transmitted 74 Transactions. light, and this colour is due to these granules, which are yellowish-brown in colour. They look like droplets of fat. Possibly this structure repre- sents the hypobranchial gland, which, as Lang mentions, is absent in all pulmonates except AmpMhola. This peculiar and striking phenomenon was met with in every specimen examined. The heart lies at the base of the left side of the kidney : its wall is formed of a thin, but tough, transparent membrane. The auricle is much smaller than the ventricle, and broader posteriorly than at its anterior end. Its wall is very thin, white, and but feebly muscular. The ventricle is yellow in colour, and its wall is more muscular than that of the auricle. The lung {I) is situated between the kidney and the anterior muscular edge of the mantle (fig. 3). The blood-vessels traversing it are not clearly visible, on account of the fact that they have very large cavities and extremely thin walls. Owing to the small size and very delicate walls of the auricle I was unable to inject the lung through the auricle, but I succeeded in injecting it through the pedal sinus, as will be described in the account of the circulatory system. It is probable that dermal respiration plays as important a part as lung respiration, and the thick layer of pigment covering the mantle in the region of the lung may act as a respiratory pigment, as may also the pigment covering the other parts of the body. Alimentary System. (Fig. 3.) The mouth [m) is placed between the two lappets of the head, and opens into the cavity of the buccal mass. It is dark in colour, somewhat ovoid in shape, the posterior portion being swollen. From the ventral surface of this posterior portion the radula-sac extends backwards for a short distance below the oesophagus. There is no jaw, nor did I find any trace Fig. 4. — Portion of the radula ( x 700). tc, central teeth ; tl, lateral teeth ; tm, marginal teeth. of a rudiment of one. Two similar and symmetrical muscular masses pro- ject into the cavity of the buccal mass in front of the radula, one on each side of the middle line. They are dark in colour, and each is simply a muscular thickening of the wall of its respective side. The radula is spatulate in shape, the pointed end being anterior. There are forty-four rows of teeth, the rows being set obliquely to the median Farnie. — The Structure of Ampliibola ci'enata Martyn. 75 line. If the radula is mounted whole, only two kinds of teeth are visible, as it is very difficult to spread it out flat, but if separated with needles three distinct kinds can be distinguished (fig. 4) — (1) central, (2) lateral, (3) marginal. The central tooth {tc) has a broad base, bearing a median cusp which is almost scpiare in outline. On either side of this are a number of smaller cusps, six or seven, but the number differs with each central tooth and often on the two sides. The cusps next to the median on either side are smaller than those more remote ; but all taper to a sharp point. On either side of the central tooth, and placed slightly above its upper margin, is a small elongated lateral tooth {tl) which is somewhat blunt at the tip. Next to this is another lateral tooth, of larger size, wdiich bears two cusps. The division into cusps is not the same in every tooth. Some have a large outer cusp and a very small, narrow inner one ; in others the cusps are of equal length and breadth. But this difference is due probably to some being more worn away than others. The remaining teeth on each side of the laterals are the marginals {tyn). They are all curved, simple, conical teeth, the tips of which are somewhat rounded. Hutton (1879) describes only two kinds of teeth in the radula of Amphi- hola — median and lateral. He also says the apices of the teeth point for- ward. He gives a very rough sketch of the radula, but the shape is not correct. In his second paper (1882) he redescribes the teeth. He notes that the median tooth hks five or six cusps on either side, not two or three as he formerly thought ; that there is a single lateral tooth, which is often divided into two and varies in shape ; and that the rest of the teeth are aculeate, and increase in length towards the margin. The form and great size of the median tooth in Amphihola seems unusual among pulmonates, for, judging from figures of radulas of other pulmonates (Bronn's Thierreich, pi. xcv) — e.g., SipJionaria, Limnaeft, Planorbis, Auricula — the median tooth is much smaller and simpler than those on either side. Perrier (1897) says that the form of the lingual teeth is related to diet : that they are obtuse and generally numerous in herbivorous molluscs, but have the form of a hook and are less numerous in carnivorous genera. The teeth in Amphibola, therefore, agree with those of other herbivorous molluscs. A pair of salivary glands open into the buccal cavity (fig. 3, sg) near the commencement of the oesophagus. Each gland is a long, linear, yellow, sacculated structure, which passes through the nerve-collar and runs for a short distance backward beside the oeso])hagus. Posteriorly they ta])er, and are attached together and to the wall of the oesophagus. The oesophagus extends backwards for about two-thirds the length of the body. The posterior portion lies beneath the intestinal coil, and is visible by transparency on the ventral surface of the uninjured animal. As far as the intestinal coil the oesophagus is a narrow tube, but it then dilates a little, the dilatation being marked off from the portion in front and behind it bv constrictions. This specialized portion of the oesophagus is the crop (c). Behind the crop the oesophagus becomes broader, and on a level with the posterior end of the intestinal coil it bears a finger-shaped diverticulum on the right side [cliv). Behind this diverticulum the oeso- phagus becomes broader, and opens into the stomach {st), which is U-shaped, the right limb being much smaller and narrower than the left, which extends forwards towards the heart. An outgrowth of the left limb of the 76 Transactions. stomach forms the gizzard {gz), which consists of two globular and sym- metrical muscular projections separated by a muscular girdle. If the stomach be opened and its wall examined, two folds of the epithelium in the form of a pad will be seen on its floor, one behind the entrance to the gizzard and the other just in front of it. From each of these two pads a white wavy fold runs along the floor of the stomach towards the intestine. Another wavy fold is present to the right of these two. The stomach passes into the intestine {int), which, after running under- neath the aorta on the left side of .the body, crosses the median line and then forms the intestinal coil. The intestine is very long, measuring in some specimens 8| in. when uncoiled. It is coiled round and round the albumen- gland (ag) in a double spiral, the total number of complete coils being eight, only five of which are visible on the surface. It coils four times from right to left, the fourth coil crossing the middle of the albumen-gland trans- versely. After coiling four times in the opposite direction it runs along the right side of the first coil and passes into the rectum. The coils from left to right alternate with those from right to left. The rectum (r) runs along the right side of the body, and opens by the anus into the triangular groove already mentioned. The extremely long coiled intestine is characteristic of herbivorous gasteropods. Amphihola has to pass through its alimentary canal enormous quantities of mud in order to obtain the vegetable matter it requires. Examination of the contents of the stomach and the mud itself shows that the food consists principally of diatoms. Several difierent kinds were found, the most frequent being Navicula. The faeces are deposited in long circular strings. Hutton's drawing (1879) of the gizzard and stomach is not quite correct ; and he says there are only five coils in the intestine, all reversed. He draws the triangular groove into which the anus opens as if it formed part of the wall of the rectum itself. The digestive gland (fig. 3, dgl) is very large, occupying together with the gonad the hinder end of the body, and extending from the region of the stomach up to the apex of the visceral spire. It occupies the median portion of the spire, and lobes extend to the edge alternating with those of the gonad. It is a much-lobed gland, dark brown in colour, and when examined fresh it is seen to be dotted with numerous brown specks, the so-called entochlorophyll granules. The duct of the liver, which appears to be single, opens into the right limb of the stomach, near its anterior end (Id). The cells lining the lumen of the liver are long columnar cells, but they are of varying lengths, some extending a considerable distance into the cavity, others being very short. Two kinds of cells are distinguishable, (a.) Liver cells : The large cells mentioned above, as well as smaller liver cells, contain small granules, which give the yellowish-green colour to the fresh liver. They stain pink in eosin. (b.) Ferment cells : These occur in amongst the liver cells, and each has a large cavity containing a yellowish- brown granule. These entochlorophyll granules can be seen at various stages of formation, some cells containing minute granules, others granules a little larger, others again very large granules. I tried several tests for these granules, with the following results : They turned red when treated with gentian violet, turned pale green when treated with methyl green, remained brown when treated with osmic acid, and turned dark green when treated with eosin. Acetic acid had no effect ; but they dissolved in caustic potash. Farnie. — The Structure of Ampliibola crenata Martyn. 77 These entochlorophyll granules are just as numerous in a fasting animal as in one that has been feeding. The only difference I found was that the granules from a fasting animal dissolved in caustic potash at once ; those in the other animals took a long time, some of them not dissolving at all. Schneider (1902) distinguishes three kinds of cells in the liver : (a) liver cells, (&) excretory cells, (c) lime cells. According to him, two sorts of granules occur in the " liver cells " — small liver-granules, which stain red in eosin, and large excretion granules (entochlorophyll). The " liver cells." he says, perform a nutritive and secretory function. The " excretory cells," he says, stain a deep black in osmic acid. The " lime cells " contain phosphate of lime. The liver cells, as I have described, are present in the liver of Amphi- hola, I tested for " excretory cells " with osmic acid, but obtained no result ; and of " lime cells " I could find no trace. MacMunn (1900) regards the cells containing entochlorophyll in molluscs as " ferment cells." He also describes " lime cells," but finds no trace of the so-called " excretory cells." He tested for glycogen in the liver, but obtained no results. Nor have I found any trace of glycogen in these cells in Amphibola. The Nervous Sy stein. (Fig. 5.) The nervous system consists of a ring of nerve-tissue surrounding the buccal mass a short distance from its posterior end. The ganglia are bright-orange in colour. The cerebral ganglia are connected by a fairly stout cerebral commissure. From each there passes backwards and downwards a slender connective to the buccal ganglia, which are, as usual, of small size, and are situated slightly behind the entrance of the salivary gland. From the buccal ganglia, whicli are joined by the commissure, small nerves are given off to the buccal mass. From each cerebral ganglion the following five nerves are given off to the anterior region of the head : («) A very fine nerve, which runs along- side and close to the buccal mass, innervates the head lappet in the region of the mouth ; (6) to the outer side of this is a nerve which almost at once bifurcates ; (c) a very fine nerve, and {d) a stouter one which bifurcates (these two run parallel with the posterior branch of nerve b) ; (e) the two tentacular nerves run outwards and slightly upwards to enter the base of each tentacle, and one of the two innervates the eye. From the right ganglion there also arises a stout nerve (/) which runs outwards and backwards and then bifurcates, the two branches supplying respectively the anterior and posterior portions of the penis. There is no corresponding nerve on the left side of the animal. The pleural ganglia lie on the body- wall close to the cerebral, to whicli each is connected by the cerebro-pleural connective. There are apparently no nerves given off by these ganglia, but from the right pleuro-pedal con- nective, and nearer to the pedal than to the pleural ganglion, a slender nerve is given off which bifurcates almost immediately ; the anterior branch (g), crossing below the penis, goes to the anterior end of the common genital duct, the posterior supplies the body-wall. On the left side the corresponding nerve, which also bifurcates, is, of course, entirely limited to innervating the body-wall of this side. The pedal ganglia are of about the same size as the cerebral ; the pleuro-pedal connectives are very short. From the pedal ganglia several large nerves supply all regions of the foot. 78 Transactions. The only really interesting feature about the system relates to the character of the visceral loop, which is much longer in Amjjhihola than in ordinary pulmonates. From the right and left pleural ganglia a connective passes back to the visceral ganglion {gv), which is situated on the body- wall below the oesophagus, slightl}^ to the right side. It is about the same size as one of the pedal ganglia, and, as we shall see later, probably repre- sents the fused infra-intestinal and abdominal ganglia. From it are given off two strong nerves. The anterior one (k) runs out to the right side, ventral to the common genital duct, and bifurcates, one branch running up to supply the inferior pallial lobe, and the other backwards alongside the rectum. The posterior nerve [1) is stout, and runs backwards to supply the organs in the visceral spire. a Tig. 5. — The nervous system in situ ( X 4). a, first cephalic nerve ; d, fourth cephalic nerve ; /, penial nerve ; g, nerve of genital duct and body-wall ; /;, nerve to osphradial ganglion (which is represented in outline as it lies on the roof) ; j, nerve to body- wall ; k, rectal nerve and its branch to the inferior pallial lobe ; /, visceral nerves ; tn, n, nerves to body-wall ; cd, common genital duct ; ce, cut edge of mantle ; gac, accessory ganglion ; cjos, osphradial ganglion ; gsi, supra-intestinal ganglion ; gv, visceral ganglion ; i^e, penis ; r, rectum ; t, tentacle. A short distance from the pleural ganglia the visceral commissure bears two ganglia asymmetrically placed, the one on the right {gsi) being larger and farther removed from the pleural ganglion than the one on the left {gac). The right one may be termed the supra-intestinal, and from it are given off two nerves. The osphradial nerve {h) runs outwards to the osphradial ganglion, which is situated on the mantle on the right side. The osphradial ganglion itself gives off small nerves to the osphradium and the mantle. A slender nerve {j) supplies the body-wall. Farnie. — The Structure of Ainphibola crenata Martyn. 79 Tlie ganglion on the left is evidently an accessory ganglion {gnc) which corresponds to that found on the visceral commissure in Ckili)ia (Lang, 1900, p. 220; and Naef, 1911). This accessory ganglion sends off a nerve (n) which supplies the body-wall in the region of the collar. Between this accessory ganglion and the visceral ganglion, but nearer the latter, a nerve (m) arises from the visceral commissure and supplies the columellar muscle. There is no ganglion corresponding to this nerve, though perhaps it arises from cells in the accessory ganglion. According to Pelseneer (1906), " In all Euthyneura except Actaeon, Ghilina, and Latia the infra-intestinal ganglion is fused with the abdominal in such a manner that the latter appears to participate in the innervation of the mantle — i.e., inferior pallial lobe." Although we find that the inferior pallial lobe in Amphibola is innervated by a nerve from the visceral ganglion, yet serial sections across the latter give no indication of the union of two such ganglia. In another primitive pulmonate, Latia, however, as figured by Pelseneer (1906) the approximation of the ganglionic centres has not gone so far, so that the infra-intestinal ganglion, although very close to the abdominal, has not fused witli it. Latia, like Afnphibola, has an accessory ganglion near the left pleural. The nervous system in Latia enables one to see how the condition in Amphibola may have come about. The comparison of the nervous system of Limnaea, Chilina, and Amphi- bola will show more clearly that the visceral ganglion in the last probably represents the fused infra-intestinal and abdominal ganglia. Button's description and figure of the nervous system do not agree with what I have found to be the case. He says that in addition to the cerebral and pedal ganglia there is " a parieto-splanchnic system, which consists of seven ganglia, three on each side, and an azygos infra-oesophageal ganglion connected with the others on either side."' The anterior ganglion of his parieto-splanchnic system corresponds to the pleural ganglion ; the posterior one to the accessory and supra-intestinal respectively ; but I find no trace of the middle ganglion on either side. He observes no dift'erence in size in these two ganglia, nor their asymmetry ; nor does he mention any buccal ganglia. Nothing is said as to the various nerves themselves. Sense Organs. — Tactile organs are distributed all over the surface of the head and foot. This is evident by the sensitiveness exhibited when the animal is touched, and also by the rich nerve-sujiply, especially in the anterior margin of the head. A slatoci/st (or otocyst) is present on each pedal ganglion. It is an oval vesicle, and contains numerous calcareous lenticular statoliths. When examined fresh the statoliths oscillate in the fluid present in the vesicle. These movements cease after a short time. Some of the statoliths lie on the base of the nerve which leaves the statocyst. This nerve is seen running close against the cerebro-pleural connective, so that one may con- clude that the nerve of the statocyst comes from the cerebral ganglion. The osphradium, is a simple epithelial ridge on the roof of the mantle- cavity close to the collar, near the pulmonary aperture (fig. 3, os). A nerve can be seen supplying it from the osphradial ganglion, which is in its turn innervated from the supra-intestinal ganglion. Hutton (1879) figures and describes the statocyst, but makes no mention of the osphradium. The ej/e, as sections show, presents no peculiarity in structure ; it is quite typically constructed. When a tentacle is mounted entire the eye 80 Transactions. exhibits two distinct portions — a small linear light area, which represenfe the lens ; and a deeply pigmented region, surrounding this but for its anterior end, is the retina (fig. 7). Below the eye, embedded in the sub- stance of the tentacle, may be seen a mass of rounded particles of carbonate of lime such as occur throughout the tissues of the body. Circulatory System. (Fig. 3.) The only portion of the circulatory system that needs describing is the venous system. In order to trace out the veins I injected the animal through the foot. The best results were obtained with glycerine carmine, and the kidney was invariably well injected. The blood is collected into sinuses, as can be proved by thus injecting the animal. From the larger sinuses the blood passes into two main tubular sinuses or veins, the anterior sinus and the rectal sinus (fig. 3). On the left side the blood from the body enters the anterior sinus {as), which lies along the collar. Shortly before reaching the pulmonary aper- ture it curves round to connect with the pulmonary vein {pv), which runs close beside the kidney, to enter the anterior end of the auricle. The anterior sinus gives afferent branches to the lung {I) along its whole course, and the blood is collected by efferent branches which enter the pulmonary vein. Thus, though some of the blood enters the pulmonary vein directly from the anterior sinus, most of it reaches the heart only after filtering through the vessels of the mantle-roof, which constitutes the lung. The rectal sinus consists of two superposed channels, one above the other — the inferior rectal sinus {irs) and the superior rectal sinus {srs). The inferior rectal sinus commences at the inferior pallial lobe, and runs along the floor of the mantle on the right side of and close to the rectum. It extends back as far as the coils of the intestine, where it leaves the body- waU floor of the mantle-chamber and, bending abruptly on itself, passes forward along the roof of the mantle above its former course as the superior rectal sinus [srs) as far as the pulmonary aperture. It then bends at right angles and traverses the mantle as far as the commencement of the collar, where it seems to cease. The blood, which enters both ends of the rectal sinus, is carried through vessels traversing the mantle from the sinus to the afferent renal vein, which runs along the dorsal surface of the kidney, and which is therefore not shown in the drawing. The blood from the afferent renal vein is then distributed through the sinuses in the connective tissue which supports the filiform papillae of the kidney. These trabeculae of connective tissue are traversed by axial sinuses which function as blood- spaces. The blood thus reaches the efferent renal vein, which runs back- wards near the ventral surface of the kidney, below the muscle-band, to enter the auricle. I have had great difficulty in tracing out the circulatory system. The heart and blood-vessels have such extremely thin walls that it is impossible to inject them from the heart. On one occasion the injection went from the auricle along the pulmonary vein and into the anterior sinus directly for a short distance, but I did not observe any injection on the wall of the lung itself. By injecting through the foot the kidney was invariably well injected, and sections across the lung showed that the vessels of the lung had also been injected. As explained above, the afferent and efferent 'vessels on the wall of the lung are not as clearly visible in Amphibola as in Helix and in other pulmonates. The same is true of the vessels running Farnie. — Thr Struct urt of Aniphibola crenata yiartyn. 81 from the superior rectal sinus to the renal vein. Sections across the mantle between the kidney and the rectal sinus, however, show the existence of these blood-vessels. The rectal sinus where it traverses the roof of the mantle is very con- spicuous. Quoy and Gaimard (1832) draw it as if it were coming from the ventricle. Hutton (1879) says it does not come from the ventricle, as Quoy and Gaimard figure ; but he was unable to trace its connection, nor does he seem to have traced out the circulatory system at all. When the animal is opened by cutting along the right side of the mantle the rectal sinus is necessarily cut across at its hinder end where it bends upwards on to the roof of the mantle. I am not c{uite certain whether the superior rectal sinus ends, as shown, near the collar (fig. 3), but I can trace it no farther. Although the rectal sinus in Amphibola is a definite blood-vessel, I have called it a " sinus " in order to compare more easily the circulatory system with that of a ty])ical pulmonate — e.g., Helix. The superior rectal sinus, then, evidently corresponds to the so-called rectal sinus of Helix, the inferior rectal sinus being an additional vessel. The circulation of blood in the lung and in the kidney agrees with that found in Helix, except that in Amphibola, as in other primitive forms, the blood after being purified in the kidney enters the heart directly. Reproductive Organs. (Figs. 3, 6.) Amphibola, like all the Euthyneura, is hermaphrodite. The genital organs lie for the most part on the right side of the body, and comprise the hermaphrodite gland (or ovotestis), albumen-gland, and an undivided genital duct, into which open certain accessory organs. The genital aperture is situated at the base of the right tentacle (fig. 2), and presumably serves for the exit of both ova and spermatozoa, though I have been unable to trace the course taken by the ova in their passage to the exterior. The ovotestis {hgl), together with the liver, occupies the visceral spire. On the ventral surface it is plainly seen as a light-yellowish-brown organ extending the whole length of the spire and embedded in the dark-brown gastric gland. On the dorsal surface, however, only portions of the gland are visible, separating the darker bands of the liver (fig. 3). It con- sists of several lobules, each composed of numerous acini, the ends of which are tipped with a dark-brown pigment. These lobules communicate with small ductules which unite to form the hermaphrodite duct (M). Posteriorly it is of a rich brown tint, but anteriorly it becomes paler till it is white. This leaves the ovotestis as a very wavy duct, wdiich passes for- ward on the ventral surface of the visceral spire to open into the common genital duct (cd). Just before the point of entrance it gives oS a small finger-shaped diverticulum, the seminal vesicle (sv), which underlies the duct and rests close against the albumen-gland. Pelseneer (1895) in a paper discussing the origin of hermaphroditism in the MoUusca refers to Aniphibola in these terms : " The wall of the genital gland shows distinct sexual difterences upon the two sides of the follicles, in which the female side exhibits projections which are rudiments of the acini of this sex." It will be remembered that Cottrell (1911) shows that in Siphonaria the peripheral acini or follicles produce only eggs, whereas the central ones produce spermatozoa. In Helix each follicle produces both kinds of germ cell from any part of the epithelium. My own observations tend to show that Pelseneer's statement is correct, except that I do not find 82 Transactions. any " projections " from the side of the follicles. Sections across the ovotestis of AmpJubola show that ova and spermatozoa are developed in the same follicle. The spermatozoa, however, are confined to one jiortion of wall, while from the rest of the epithelium the ova are formed. They develop at a later period of the year. Spermatozoa are fully developed in November, whereas at this date the ova are still small and not ready to be discharged. The common genital duct consists of two di.- tinct regions — (a) glandular, (6) non-glandular. The glandular region (gld), into which the hermaphrodite duct leads, lies in close contact with the posterior ventral portion of the Pio (;_ — The genital system unravelled so as to exhibit as mueh as possible ( X 2). The point of entrance of the prostate into the cavity of the penis is indicated by dotted lines, ag, albumen- glanci ; cd, common genital duct ; gld, glantlular portion of common duct; gp, genital pore; hd, hermaphrodite duct; hgl, hermaphrodite gland; pe, jienis ; pr, prostate; sv, seminal vesicle. albumen-gland (og). It is a white, mucilaginous, finely coiled tube, all the coils of which I have not attempted to show in the drawing. This tube gradually loses its mucilaginous character and widens to form the com- mencement of the non-glandular portion (cd), w^hich narrows again as it passes forward along the body-wall parallel to, and on the left of, the rectum as a wavy duct of a cream colour. It reaches almost to the base of the right tentacle, narrowing slightly as it does so. It then turns sharply on itself, runs backwards, and after a short distance bends abruptly and becomes much enlarged to form the penis (pe), which is a pyriform organ of a light-cream colour with very muscular walls. Farnie. — Tht Structure of Amphibola crenata Marfi/n. 83 Opening into the common duct are two diverticula, the albumen-gland and the prostate. The albumen-gland {ag) opens into the distal end of the glandular region opposite the point at which it passes into the non- glandular. It is a brownish or orange-coloured tubule, which is very much convoluted, as Hutton described, and forms a spherical mass, around which are wound the numerous coils of the intestine. It is soft and of a somewhat slimy consistency, and its cells secrete a great quantity of mucilaginous material. At the commencement of the penis is .situated the prostate (pr). It is a much-convoluted blindly-ending tube, the distal half pure-white in colour, the proximal half bright-yellow. From this end a slender duct leads away, which, after running in the substances of the muscular wall of the penis, communicates with its cavity near its opening to the exterior. From the above description it will be seen that the condition of the genital duct in Amphibola agrees with the most primitive condition in the Euthyneura — that is, the duct is a sperm-oviduct throughout its length. To this type of duct Lang (1900) and Pelseneer (1906) give the name " monaulic." As far as I can ascertain, the only other primitive pulmonate closely related to Amphibola which exhibits a monaulic type of duct is Siphonaria. Cottrell (1911) shows that the reproductive organs of this genus differ from those of Amphibola in three chief features : There is no separate albumen- gland, but the common duct is itself glandular, and the much-folded walls of this duct constitute the albumen-gland ; the common duct enters the penis close to its external pore and not at its distal extremity ; and there is a large spermatheca, the long duct of which opens into the penis close to the common duct. The absence in Amphibola of a distinct and definite spermatheca seems a peculiarity. Limnaea, which has affinities with Amphibola, has a " diaulic " type of genital duct which cannot be compared with that of Amphibola. In Chilina, another primitive pulmonate, the reproductive system of which Lang (1900) figures and describes, the genital duct is " diaulic," the open- ings of the sperm-duct and oviduct being at some distance from each other. Considering the close relationship of Amphibola and Chilina, one would have expected a greater similarity in their reproductive systems. Quoy and Gaimard (1832) described the reproductive system of Amphibola. They called the hermaphrodite gland the " ovary," and the hermaphrodite duct the " oviduct." The albumen-gland they named " testicule," and the genital duct which runs up on the right side the " uterus." The opening of the female portion of the duct they figure on the right side of the body, to the left of the anus. The penis they describe as opening near the eye. in the place where the right tentacle would be if it were represented in the figure. Hutton (1879) correctly describes the hermaphrodite gland and the hermaphrodite duct. The albumen-gland he says consists of two parts — an albumen-gland proper and an accessory gland. The albumen-gland proper opens into the hermaphrodite duct by a duct. According to him, the hermaphrodite duct appeared to divide beyond the albumen-gland into a large sacculated " oviduct," and a narrower but still broad " vas deferens" (which is the "common duct" of my account), but , he could not satisfy himself as to how the oviduct left the hermaphrodite duct. He describes it as running along the left of the rectum, to which it is firmly attached. " It appears to open inside the respiratory cavity," but of this he 84 Transact ions. ! says he was by no means certain. In a later paper (1882) he says he found an animal with the oviduct distended with eggs, and it showed clearly that his supposed " accessory gland " was the commencement of the oviduct. I can find no opening of a female duct in the position figured by Quoy and Gaimard, nor do I find any oviduct as described by Hutton. What he supposes to be the commencement of the oviduct is the lower end of the genital duct ; and serial sections in this region prove this to be so. Sections across the right side of the body show no trace of a duct between the rectum and the genital duct, whereas sections across the genital duct itself show the existence of a deep fold in its wall, which serves to divide the duct into two portions, presumably, during the passage of the ova and spermatozoa. Hutton (1879) says the eggs of Amphibola are " lodged on the exterior of the mantle in a circular patch near the opening of the renal organ. After fertilization they acquire a thick coat which gives them a bluish- white pearly appearance." These are evidently the fluorescent particles I described in connection with the kidney, where I mentioned that they were products of the hypobranchial gland. They are not eggs, as I have observed them in every animal without exception that I have examined during the year. Moreover, they do not resemble eggs in the slightest degree. In his second article (1882) Hutton says he found the oviduct so distended with eggs that he was able to trace its connection with the hermaphrodite duct. The "eggs" he found in the oviduct were, I think, the eggs of a parasitic Trematode. I have found them several times, and in some animals they are so numerous on the right side in the muscular region of the body-wall between the rectum and the genital duct that both the rectum and the genital duct are hidden from view — i.e., in the position of Hutton's supposed '" oviduct." At present I am making systematic observations on Amphibola so as to ascertain at what time the ova are laid and how they get to the exterior. Every month I collect and preserve the animals in order to cut sections of the reproductive organs and ascertain at what time of the year the eggs are laid. If successful I shall try to follow out the development of the eggs as far as possible. Fig. 7. — The end of a tentacle, with the eye, cleared and mounted entire, c, carbonate of lime ; I, lens; p, pigment ; /, tip of tentacle. Embedded in the connective tissue and amongst muscles in all parts of the bod}', are numerous bodies composed of carbonate of lime. They are extremely abundant, especially on the mantle-edge. They vary in size, the smallest ones being found embedded in the base of the tentacle below the eye (fig. 7). They vary in shape also, some being spherical, others Farnie. — The Strticture of Amphibola crenata Marfyii. 85 ovoid, and others again more or less rhomboidal. Examined under the high power some exhibit fine circuLar striations. When treated with acetic acid they dissolve, giving off large bubbles of carbon dioxide, which can be plainly seen with the naked eye. Bibliography. BouviER, E., 1892. Sur I'orgamsation des Amphiboles, Bull. Soc. Pliilom. Paris, 8, vol. 4. Cooke, A. H., 1895. Cambridge Xatural History, MoUusca. COTTRET.L, A. J., 1911. Anatomy of Siphonaria obliquata (Sowerby), TraMs. N.Z. Inst., vol. 43, pp. 582-94. HuTTON, F. W., 1879. Aim. Mag. Nat. Hist., ser. 5, vol. 3, p. 181. HtTTTOK, F. W., 1882. Tranc. N.Z. Inst., vol. 14, p. 156. Lang, A.. 1900. Lehrbuch der vergleichenden Avatomie. d. unrbellose Thiere (2nd ed.), Mollusca, by Karl Hescheler. MacMunn, C. a., 1900. On the Gastric Gland of Mollusca and Decapod Crustacea, Phil. Trans. Roy. Soc, vol. 193b. Naef, a., 1911. Studien z. generellen Morphol. d. Mollusken, in Spengel's Ergebnisse u. Forischrifte d. Zoologie. Pelseneer, p., 1895. Hermaphroditism in Mollusca, Quart. Journ. Micr. Sci., vol. 37, p. 19. Pelseneer, P., 1906. Mollusca, in Lankcster's Treatise on Zoology. Perrier, E., 1897. Traite de Zoologie. QuoY and Gaimard, 1832. Voyage de V Astrolabe, vol. 2, p. 196 ; pi. 16, figs. 1-9. .Schneider, A, 1902. Lehrbuch d. vergleich. Histologie d. Thiere, p. 570. SuTER, H., 1913. Manual of the Neiv Zealand Mollusca, pp. 596-97, Wellington. SuTER, H., 1915. Manual of the New Zealand Mollusca, Atlas of Plates, pi. 49, figs. 9, 9a, Wellington. Art. IX. — Contributions to a Fuller Knowledge of the Flora of New Zealand : No. 6. By T. F. Cheeseman, F.L.S., F.Z.S., Hector Memorial Medallist, Curator of the Auckland Museum. [Read before the Auckland Institute, 20th December, 191S ; received by Editor, 30th December, 1918 ; issued separately, 14th May, 1919.] I. Kanunculaceae. The Genus C'altha in the Southern Hemisphere. A memoir bearing the above title, written by Captain A. W. HilL Assistant Director of the Royal Gardens, Kew, has recently appeared in the Annals of Botany (No. cxxvii, July, 1918). In this, Captain Hill main- tains the subdivision of the genus into the two sections, Psychro]}hila and Pojndago, proposed by de Candolle as far back as 1818, and shows that the peculiar development of the leaf-auricles in PsychrophUa, which includes the whole of the species found in the Southern Hemisphere, marks off the section much more distinctly than the floral characters proposed by de Candolle. Eleven species are included in the section, three of them being described for the first time. Seven of the eleven are purely American in their distribution, two of them advancing as far north as the Andes of Ecuador or Bolivia ; the remaining five extending southwards into southern 86 Transactions. Chile or Fuegia, two of them reaching the Falkland Islands. Four species are Australasian, one being found in Victoria, another in Tasmania, and two others (C. novae-zealandiae Hook. f. and C. ohtusa Cheesem.) in New Zealand. Much information is afforded for the first time respecting the degree of development of the leaf-auricles, and woodcuts are given of the chief modifications, the leaves of both the New Zealand species being figured. It is worth remarking that the section Psychrophila is one of those plant- groups proving an alliance between the floras of Australia, New Zealand, and South America. XVIII. Ehamnaceae. Pomaderris elliptica Lab. Kawliia district, growing luxuriantly on the fern-clad spurs and pro- montories running down into the harbour ; Mr. E. H. Schnackenherg / An extension of the southern range of this fine plant, the northern slopes of Mount Pirongia being the previous known limit. XXII. Leguminosae. Chordospartium Stevensoni Cheesem. Avon Valley, Marlborough ; H. F. Hursthouse ! This is a most inter- esting discovery, the plant being previously known only from the original habitat near the Clarence Bridge, South Marlborough, where it was collected by Mr. George Stevenson in the summer of 1909. Mr. Hursthouse informs me that in the Avon Valley it grows side by side with Notosjmrtnmi Car- micJiaeliae, and that it is very difficult to distinguish the two in the absence of fruit. He further remarks that when in bloom both are very beautiful and striking plants, certain to attract notice even at a distance of half a mile or more. Mr. Hursthouse has also favoured me with a large supply of the seeds of Chordospartium. It seems to be difficult of germination, for out of great numbers planted, both inside and outside New Zealand, only three plants have been reared. XXVIII. Myrtaceae. . Metrosideros Parkinsoni Buchanan. Abundant at the southern end of the Paparoa Range, near Greymouth. Particularly plentiful on the steep slopes south and south-east of Mount Sewell, and also on a spur running to the west of Mount Davy, alt. 2,000 ft. ; P. G. Morgan ! The above are the most southern localities yet recorded for this fine plant. I have also to record its discovery by Mr. W. R. B. Oliver on the summit of Mount Hobson, Great Barrier Island, alt. 2,000 ft. The two specimens kindly given to me by Mr. Oliver have rather narrower leaves than the southern examples, and there are fewer flow^ers in the cymes, but otherwise they entirely correspond. Its occurrence on the Great Barrier Island, quite 350 miles in a straight line from the nearest of its southern habitats, is a remarkable instance of discontinuous distribution, almost comparable to the case of Pittosporum ohcordatum, where the only two localities known — that of Kaitaia, in Mongonui County, and Akaroa, in Banks Peninsula — are separated by 550 miles ! Cheesema>\ — ('onfributio)is to Knowledge of Flora of N.Z. 87 XXXIII. Umbellipeeae. Aciphylla similis Cheesem. Griffin Range, western Southern Alps, alt. 4,500-4,900 ft. ; P. G. Morgan ! The Griffin Range is situated almost immediately to the south of the Otira-Kumara Road, and a little distance below the point of con- fluence of the Taipo and Taramakau Rivers. It has never been previously visited by a botanist, and I am consequently much indebted to Mr. Morgan for the few specimens he was able to secure during a hasty geological examination of the district. Aciphylla Kirkii Buchanan. I am indebted to Mr. James Speden, of Gore, for excellent specimens of this curious plant, collected at an altitude of 6,000 ft. on the Remark- ables, near the lower end of Lake Wakatipu. Mr. Buchanan's plate and description, given in Trans. N.Z. Inst., vol. 19, p. 214, are far from correct ; but they were admittedly founded on very imperfect material. In a memoir on Aciphylla, now in course of preparation, I hope to publish an amended description of this and other species of the genus. Aciphylla simplex Petrie. I have also to thank Mr. Speden for flowering specimens of this, also gathered at an elevation of 6,000 ft. on the Remarkables, near Lake Wakatipu.. XXXVII. RUBIACEAE. Coprosma tenuicaulis Hook. f. Tuamarina Swamp, near Blenheim, Marlborough, abundant ; J. H. Macmahon I So far as I am aware, this is the first record of the occurrence of this in the South Island. XXXVIII. COMPOSITAE. Celmisia Walkeri T. Kirk. Several localities on the Humboldt and Eyre Mountains., Central Otago ; J. Speden ! Celmisia ramulosa Hook. f. Eyre Mountains, Central Otago, alt. 5,000-6,000 ft. ; J. Speden ! Celmisia lateralis Buchanan. Mount Davy, southern end of the Paparoa Range, near Greymouth, alt. 2,500-3,000 ft. ; P. G. Morgan ! This species has a pre-eminently western distribution, and is seldom seen on the eastern side of the dividing range. Celmisia prorepens Petrie. Eyre and Garvie Mountains, Central Otago ; J . Speden ! 88 Transactions. Celmisia dubia Cheesem. Abundant on Mount Davy, southern end of the Paparoa Range, near Greymouth, alt. 2,500-3,000 ft. ; P. G. Morgan ! This locality offers a slight extension of the southern range of this plant. Helichrysum grandiceps Hook. f. Griffin Range, western Southern Alps, alt. 4,500-4,900 ft. ; P. G. Morgan ! Abrotanella linearis Berggren. Slopes of Mount Davy, southern end of the Paparoa Range, near Grey- mouth, alt. 2,500-3,000 ft. : P. G. Morgan ! XLI. Campanulaceae. Pratia perpusilla Hook. f. Marlborough — Wairau River bed, near its mouth ; J . H. Macmalion ! The first specimens I have seen from the South Island ; but it is easily overlooked, and probably has a wider range than is generally svipposed. XLIII. Epacridaceae. Dracophyllum Kirkii Berggren. Griffin Range, western Southern Alps, alt. 4,500-4,900 ft. ; P. G. Morgan ! XLIX. Loganiaceae. Mitrasacme montana Hook. f. var. Helmsii T. Kirk. Abundant from a little over 2,000 ft. to the summit (3,410 ft.) of Mount Davy, at the south end of the Paparoa Range, near Greymouth ; P. G. Morgan ! This is probably the locality where it was originally discovered by Mr. Helms. I have not seen specimens from any locality outside the Paparoa Range. L. Gentianaceae. Sebaea ovata R. Br. Vicinity of Wanganui ; A. Allison! An entirely fresh locality for this rare and local plant. Gentiana patula Cheesem. Griffin Range, western Southern Alps ; alt. 4,500-4,900 ft. ; P. G. Morgan ! Gentiana bellidifolia Hook. f. Griffin Range, western Southern Alps ; alt. 4,500-4,900 ft. ; P. G. Morgan ! (with the preceding species). LIV. SCROPHULARIACEAE. Euphrasia Cockayniana Petrie. Griffin Range, western Southern Alps ; alt. 4,500-4,900 ft. ; P. G. Morgan ! Cheeseman. — C out ribut ions to Kiioirledgt of Flora of X .Z. 89 LXI. Nyctaginaceae. Pisonia Brunoniana Endl. I am informed by Mr. Robert Hustie that a small grove of Pisonia exists on Cape Bream Tail, a little to the north of Mangawai. This locality, how- ever, is not many miles distant from the Taranga Islands (Hen and Chickens), where the plant is abundant. LXII. LORANTHACEAE. Korthalsella salicornioides Van Tiegh. Queen Charlotte Sound, parasitic on Leptospermum ; J. H. Macmahon ! This is the first record, so far as I am aware, for the Marlborough Pro- vincial District. (See my list of the known localities, given in Trans. N.Z. Inst., vol. 43, p. 182.) LXXIV. Balanophoraceae. Dactylanthus Taylori Hook. f. Ranginui Range, near Mangapehi, Main Trunk Railway ; J. Corhitt ! LXXVI. Urticaceae. Urtica ferox Forst. Bay of Islands County, apparently confined to a waJii-tapu known as Ngamahanga, situated about ten miles to the west of Kawakawa ; T. H. Trevor ! This is a marked extension of the range of the species, which has not been previously collected northwards of the Marikopa River, Kawhia, quite two hundred miles away. It is (or, rather, was) abundant between the Awakino and Mokau Rivers and Taumarunui, and is known from several localities between the Main Trunk Railway and the Central Volcanic Plateau. A locality near Te Aroha, reported to me many years ago, has so far not been confirmed. Mr. Trevor states that the Ngamahanga wahi-tapu contains about 29 acres. Up to this year cattle had barely penetrated into it, but they are now working their way steadily towards the centre, and he anticijjates that they will soon destroy the major portion of the undergrowth, including the Urtica. So far as he can ascertain, it has never occupied an area much exceeding an acre. Its greatest height is about 6 ft. The specimens for- warded to me have leaves from 4 in. to 6 in. in length, and the stinging- hairs are quite copious. LXXVIII. CONIFERAE. Dacrydium Bidwillii Hook. f. Open pumice country at Tiroa, to the east of Mangapehi, Main Trunk Railway; A. Wilson and J. C. Rolleston ! With the exception of the extreme summit of Moehau (Cape Colville), this is the most northerly locality known. Mr. Rolleston informs me that the Maoris call it " Aotea." Phyllocladus glaucus Carr. Several specimens in a patch of kauri forest near Birkdale, a few miles from Auckland, on the northern side of the Waitemata Harbour ; H. B. Matthews ! Quite an unexpected discovery. I am acquainted with but 90 Transactions. two other localities in the Auckland District — one near the Waitakare waterfall, where it was plentiful until the construction of the huge dam for the Auckland water-supply destroyed most of the adjacent forest ; the other a little to the north of the mouth of the Waitakare River. Mr. E. Phillips Turner informs me that a few plants of P. glaucus exist in a ravine near the base of Rainbow Mountain, near Waiotapu ; and that it is plentiful at Lake Waikare-iti, near Waikaremoana. The latter is the most easterly locality known. LXXIX. Orchidaceae. Thelymitra pachyphylla Cheesem. To this species I refer specimens of a Thelymitra collected by Mr. H. B. Matthews between Erua and Makatote, to the west of Ruapehu. It agrees with T. pachyphylla in the broad and flat erect staminodia, the margins of which are furnished with simple or branched fimbriae ; and the size, mode of growth, and foliage are all very similar. But the flowers are smaller, and the middle lobe of the column shorter and crenulate. XCI. Cyperaceae. Kyllinga brevifolia Rottb. Abundant in swamps on the seaward side of the cliffs to the north of the Manukau Harbour ; T. F. C. In this locality it is certainly a recent introduction ; nor am I aware that it has been previously collected in New Zealand outside the North Cape peninsula. But its nativity in any part of New Zealand must be regarded as exceedinglv doubtful. Carpha alpina R. Br. Mr. P. G. Morgmt sends me a highly depauperated state from the summit of Mount Frederic, north of the Buller Valley ; alt. 3,500 ft It forms small dense patches barely more than an inch in height, and the inflorescence is reduced to one or two spikelets. XCII. Gramineae. Ehrharta Colensoi Hook. f. Griffin Range, western Southern Alps ; alt. 4,500-4,900 ft. ; P. G, Morgan ! Microlaena polynoda Hook. f. In great abundance on the site of the old Maori pa Te Korekore, near Muriwai, about twenty-five miles north of the Manukau Heads ; T. F. C. This is the only locality I am acquainted with in the Auckland District. XCIII. Filices. Asplenium japonicum Thunb. Banks of the Waiaruhia River, a tributary of the Waitangi, Bay of Islands County T. H. Trevor ! This locality is some distance to the south of the Okura River, where it was first discovered by Miss Clarke. (See Trans. N.Z. Inst., vol. 22, p. 448.) Chebseman. — Contributions to Knowledge of Flora of A .Z. 91 Naturalized Plants. Aster subulatus Michx. This plant was first noticed in the vicinity of Auckland about twelve years ago, and soon became plentiful, especially in moist places on harbour reclamations, by roadsides and ditches, &c. It is a native of the United States, where it is principally found in brackish-water marshes, ranging from New Hampshire to Florida. Erigeron annuus Linn. Has appeared in some c{uantity in freshly sown grass at Otukai, Mongonui, January, 1917 ; H. Carse ! So far as I am aware, this is the first record of the occurrence of this plant in New Zealand. Native of North America, where it has a wide range ; and it has also become naturalized in Europe. Chlora perfoliata Linn. Manuka scrub at Parengarenga, North Cape district ; W . R. B. Oliver ! Now recorded for the first time in New Zealand. It is a native of western and central Europe, extending to north Africa and western Asia. Emex australis Stein. Near Parkhurst, Kaipara ; H. P. McLeod / This species appears to be of uncertain occurrence in New Zealand, and never lingers long in any one locality. It has a wide distribution in South and Western Australia and South Africa. Tradescantia fluminensis Veil. A garden escape in many localities in the vicinity of Auckland, where it has received the local name of " wandering-jew." Has become specially abundant on portions of the Mount Eden lava-fields ; T. F. C. Mongonui County — has become plentiful on river-banks near Awanui and Kaitaia, and also covers considerable areas in flat swampy forest ; H. Carse ! Mr. B. C. Aston also informs me that it is spreading fast in the vicinity of Wellington. Native of South America, from the south of Brazil to Uruguay and Monte Video. Elodea canadensis Michx. Clear running streams near Featherston, not common ; K. W. Allison! Considering how rapidly this plant increased when first introduced into Britain, it is somewhat remarkable that its spread in New Zealand has been so slow since its first introduction in 1870. Panicum Lindheimeri Nash. Vicinity of Kaitaia, Mongonui County ; H. B. Matthews ! Originally found on the summit of a hill by Kerikeri Pa, near Kaitaia ; but it has since been observed in several localities in the district. I am indebted to Dr. Stapf, of the Kew Herbarium, for the identification. Native of North America, where it is said to be a common and widely distributed species, found in dry woods and open grounds from Maine to northern Florida, and westwards to southern California. 92 Transactions. Cynosupjs echinatus Linn. I am indebted to Mr. J. P. Kalaugher for specimens collected by roadsides at Waihi. I believe this is the first record for the Auckland Provincial District. Selaginella denticulata Link. Has been known for many years as a garden escape at Pakaraka, Bay of Islands, and has lately appeared in great abundance on the banks of several swampy creeks in the neighbourhood ; T. H. Trevor ! I am also informed by Mr. B. C. Aston that it is not uncommon in several localities near Wel- lington. As it is now firmly established in the Bay of Islands locality, its further increase may be anticipated. Art. X. — So7ne Additions to the New Zealand Flora. By T. F. Cheeseman, F.L.S., P.Z.S., Hector Memorial Medallist, Curator of the Auckland Museum. [Bead before (he AucJcland Institute, 20th December, 1918 ; received by Editor, 30th December, 1918 ; issued separately, 14th May, 1919.] 1. Ligusticum petraeum Cheesem. n. sp. Species cum Angelica decipiens Hook. f. et Ligusticum aromaticmn Hook. f. confusa, a priore fructu, a posteriore foliis et floribus diflert. Herba aromatica, 5-13 cm. alta. Radix robusta. longe attenuata, ad apicem reliquis foliorum emarcidorum vestita. Folia numerosa, diffusa, 2-5-10 cm. longa, subcoriacea aut herbacea, piunata ; petioli 1-6 cm. longi, basi in vaginam expansi. Pinnae 4-8 jugae, 5-12 mm. longae, ovatae vel ovato-deltoideae, profunde incisae ; lobis acutis vel subacutis, nunquam piliferis. Pedunculi multi, graciles, nudi, foliis longiores aub breviores. Umbellae compositae, 2-4 cm. diam., 4-8-radiatae. Involucri bracteae parvae, lineari-subulatae, basi dilatatae. Flores albi. Calycis lobi acuti. Carpella lineari-oblonga ; stylis longis, recurvis. Hab. — South Island : Abundant on the north face of Mount Owen, Nelson, alt. 4,000 ft., usually on the debris from limestone rocks ; T. F. C. Also plentiful on the southern face of the same mountain ; W. Townson ! Broken River, Canterbury Alps, alt. 3,500 ft. : T. F. C. Takitimu Mountains, Southland, alt. 3,500 ft. ; D. Petrie ! Very aromatic, 2-5 in. high. Root stout, long and tapering, clothed at the top with the bases of the old leaves. Leaves numerous, all radical, spreading, 1-4 in. long, subcoriaceous or herbaceous, pinnate ; petiole from ^ to ^ of the length of the whole leaf, broadly sheathing at the base ; leaflets 4-8 pairs, rarely more, i— | in. long, ovate or ovate-deltoid or broadly deltoid in outUne, deeply and somewhat sharply incised, sometimes almost pinnate at the base ; lobes obtuse or subacute, never hair-pointed. Flower- ing-stems or peduncles many, longer or shorter than the leaves, rather slender, not branched, naked or furnished with a small pinnatifid leaflet about the middle. Umbels compound, |-1| in. diam. ; rays 4-8, slender, unequal, J-f in. long. ; involucral bracts small, linear ; usually with a dilated base. Flowers white ; calyx-lobes rather long, acute ; styles very long, recurved. Fruit linear-oblong, J in. long, not seen quite ripe. Cheeseman. — Additions to the N t ir Zealand Flora. 93 This has much of the habit and appearance of Angelica decipien.s, and the two are easily confounded in the absence of fruit. There is also a resem- blance to some states of L. aromaticum ; but in reality it differs in habit, in the spreading leaves with their much more remotely placed pinnae, in the unbranched flowering-stems, and particularly in the acute calyx-lobes, and the very long recuryed styles. I have been acquainted with it for many years. 2. Veronica Birleyi N. E. Brown in Keiv Bulletin for 1911, p. 345. " Affinis F. spathulatae Benth., sed ramis crassioribus, foliis subsessilibus et pedunculis multo brevioribus differt." " Suffrutex nanus, 10 cm. altus, ramosus ; rami erecti, saepe flexuosi, 1-2 mm. crassi, puberuli demum sublignosi et giabri. Folia conferta vel inferiora ad 4 mm. reniota, subsessilia, crassa, 6-9 mm. longa, 4-9 mm. lata, cuneato-obovata vel orbiculata, basi plus minusve cuneata, breviter et obtuse 3-7-loba, utrinque puberula, rubrotincta. Flores pauci, magni, prope apicem ramorum axillares. Pedunculi 2-3 mm. longi, 1-2-flori, bibracteati ; bracteae 4 mm. longae, lineari-spathulatae, obtusae, glandu- loso - puberulae. Pedicelli 1-1-5 mm. iongi, glanduloso - puberuli. Calyx 4-partitus ; lobi 5-6 mm. longi, 2-5-2-75 mm. lati, oblongi, obtusi, glanduloso- puberuli. Corolla ' magna, 5-mera, alba ' (Gibbs). Capsula 5 mm. longa, 4-4-5 mm. lata, glabra, in lobos oblongos obtusos 4 disrupta." South Island : Between rocks on the top ridge of Mount Bonpland, near Lake Wakatipu, 2435 m., February, 1908 ; Aliss L. G. Gibbs (No. 1172). '' Allied to F. spathidata Benth., but differs in having much stouter branches, subsessile leaves, a finer and entirely different pubescence, and very much shorter peduncles. The corolla, according to Miss Gibbs, was white, about f in. in diameter, with 5 subequal lobes ; several were col- lected, but unfortunately they were lost. The name is given in honour of Mr. Harry Birley, a well-known guide in the district, who accompanied Miss Gibbs when this plant was collected." I must express my indebtedness to Miss Gibbs for furnishing me with one of the type specimens. Mr. Brown's description appears to have been overlooked by most New Zealand botanists, for when, a feAv years later, flowerless specimens were collected on the Copland Pass by Mr. P. Graham, Chief Guide at the Mount Cook Hermitage, they were described as a new species by Mr. D. Petrie, under the name of Veronica Grahami. {Tnins. N.Z. Inst., vol. 45, p. 273, 1913.) In March, 1917, it was again collected by Mr. W. A. Thomson and Mr. J. Speden in considerable quantity at an elevation of 5,000 ft. on Mount Tennyson, near Garston, Lake Wakatipu. An excellent series of specimens was obtained, showing that the plant attains a somewhat greater size than had been supposed, a single plant sometimes covering an area 6 in. to 9 in. across. Late in autumn the old leaves become almost glabrous, but the younger shoots are always densely puberulous. The flowers vary in size from | in. to | in. in diameter. As it seems inqjortant that the first description of this plant, and a knowledge of the original locality, should be readily accessible in the Dominion, I have placed the particulars on record herewith. 3. Earina aestivalis Cheesem. n. sp. Affinis E. mucronatae a qua differt caulibus robustioribus firmioribusque, foliis latioribus et brevioribus, floribus majoribus, labello longiore, lobis lateralibus majoribus et acutioribus. 94 Transactions. Hub. — Xortli Island : Near Ahipara, li. H. MaUJieivs 1 and at Kaiaka, H. Carse ! both localities in Mongonui County. In forest at Muriwai, and near the mouth of the Waitakare River : T. F. C. Forest by the Waikanae River, Wellington ; B. H. Morison ! Rhizome creeijing, much as in E. fniicronata. Stems numerous, 9-18 in. long, suberect or drooping, smooth, compressed, rather broader and stouter than in E. mucronata, and firmer. Leaves 3-6 in. long, i-^ in. broad, flat, stift', erect, narrow-linear, acute or acuminate ; midrib and veins con- spicuous on the under-surface, not so evident above. Panicle terminal, 2-5 in. long ; branches or racemes 3-7, rarely more, 1-1| in. long, 4-7- flowered ; bracts short and broad, clasping, many-striate. Flowers larger than in E. mucronata, | in. diam. or more. Sepals and petals similar in size and shape, linear-oblong, subacute. Lip longer than in E. mucronata, and brighter in colour ; lateral lobes wider and more acute. Column short, stouter. I have been acquainted with this plant for several years, having gathered specimens at the mouth of the Waitakare River as far back as 1895. But the differences between it and E. mucronata are mainly com- parative, and before describing it I was anxious to satisfy myself as to how far they were constant. Since then I have seen specimens gathered in several localities between the North Cape peninsula and Wellington ; and as I find that the distinguishing characters — viz., stouter and stiffer habit, broader and more rigid leaves, larger flowers, longer lip with broader lateral lobes, and stouter column — are constant throughout, I cannot any longer refuse it distinction as a separate species. In addition to the above, there is the important fact that it flowers from the beginning of Januar}^ to the first week in February, whereas the flowering period of E. ynucronata is two months earlier at least, stretching from the first week in October to the middle or end of November. At Sluriwai, a few miles to the north of the mouth of the Waitakare River, I observed it in full bloom on the 16th January, 1916 ; while typical E. mucronata growing in the vicinity had practically matured its capsules. 4. Thelymitra aemula Cheesem. n. sp. Species ad T. ixioides proxime accedit, sed differt columnae lobis lateralibus multo elongatis, et lobo mediano non cristato. Caules robusti vel graciles, 18-60 cm. longi. Folium auguste lineare, crassum, canaliculatum. Folia caulina vel bracteae vacuae 2. Flores 3-8, caerulei, in racemum 4-10 cm. longum dispositi. Sepala et petala oblonga vel ovato-oblonga, obtusa vel subacuta. Columna brevis, crassa, superne attenuata, 5-loba ; lobis lateralibus elongatis, complanatis, penicil- latis ; lobo mediano breve, dorso non cristato. Hah. — North Island : Leptospermum scrub at Birkdale, near Auckland ; H. B. Matthews! Stems stout or slender, 6-16 in. high. Leaf shorter than the stem, narrow-linear, thick, channelled in front. Cauline leaves or empty bracts 2, short. Flowers 3-8, about \ in. in diameter, blue, rather closeh' placed in a raceme 1^4 in. long. Sepals and petals oblong or ovate-oblong, obtuse or subacute. Column short, stout, broad at the base, narrowed above, winged ; the wing extending behind the anther and free from it except at the base, 5-lobed ; the two lateral lobes twice the length of the oth-ers, flattened, fringed with cilia for the greater part of their length ; middle lobe short and broad, thickened and denticulated at the tip, but smooth Cheeseman. — Additions fn the Neiv Zealand, Flora. 95 at the back ; the two intermediate lobes distinct from the central one, reaching half the height of the lateral lobes, broad, thick, and fleshy, jagged at the top. Anther broad, produced into a pointed tij) that just overtops the level of the median lobe of the colunm-wing. This interesting discovery is due to the activity of Mr. H. B. Matthews, so well known from the many additions made by him to the orchid flora of the North Cape peninsula. It is doubtless very closely allied to T. ixioides and the Australian T. canaliculata, but appears to constantly differ in the lateral lobes of the column being much longer, flattened, and more copiously penicillate ; and the middle lobe, although denticulate at the top, is not at all warted or crested at the back. The flowers appear to be invariably blue ; but the column is surrounded by a narrow band of violet just below the lobes, above which the colour is bright yellow. Art. XI. — A New Variety of Pteris macilenta. By H. Carse. [Bead before the Auckland Institute, 20th December., JOIS : received by Editor, 30th December, 1918 ; issued separately, 14th May, 1919.] Pteris macilenta A. Eich. var. saxatilis Carse var. nov. Planta decumbens vel suberecta ; quam typo in partibus omnibus minor tenuiorque Stipes 8-24 cm. longus, tenuis, canaliculatus, flavus, suffuscus vel purpureus, glaber, mfra squamosus. Frondes 10-36 cm. longae, 8-15 cm. latae, ovatae vel lanceolatae, valde membranaceae, hand lucidae ut in typo, 3-4-pinnatae. Rhachis fere filiformis. Pinnae primariae distantes, inferiores 8-18 cm. longae, adscendentes ; pinna terminalis 25 mm. longa ; segmenta ultima alte et acute dentata, apex saepe laciniatus. Sori in segmentorum sinubus brevissimi. This variety of Pteris macilenta has for years appeared to me worthy of a distinctive name. It differs from the type in many important characters, and, while occasionally forms connecting it with the type on the one hand and with var pendida on the other are seen, the usual form of this variety could not be mistaken. It is most plentiful in rather dry .situations in forests, usually where detached rocks crop up. The following are some of its main characters : The plant is decumbent or suberect, with a very short usually erect rhizome. Stipes 8-24 cm. long, slender, grooved, pale yellow, reddish-brown, or almost purple (as are the rhachises), darker at the base, quite smooth except for a few scales below. Fronds 10-36 cm. long, 8-15 cm. wide, ovate or lanceolate, very mem- branous, pale dull green, glabrous, 3- rarely 4-pinnate below ; rachis almost filiform ; primary pinnae distant, usually 6 pairs, lower opposite, 8-15 cm. long, obliquely placed on the stipes ; terminal pinnae 25 mm. long. Secondary pinnae stalked, on the lower branches again pinnate, on the upper pinnatifid, terminal ones adnate and decurrent. Pinnules 12-20 mm. long. Ultimate segments deeply and sharply toothed, the apex often laciniate. Veins free, or very slightly anastomosing along the costa. Sori in notches between the segments, very short. Hub. — Among detached rocks in hilly forests, Mongonui County, Bay of Islands, Whangarei, Manukau County : H. C. Coromandel Peninsula : H. B. Matthews ! Thames ; D. PetrieJ 96 Transactions. Art. Xll.~New Fossil Mollusca. By J. A. Bartrum, Auckland University College, [Read before the Auckland Institute, 20th December, 1918 ; received by Editor, 30th December, 1918 ; issued sejjurately, 14th May, 1919.] Plate VI [. The following Mollusca have mainly been collected from fossiliferous sands near the mouth of Kawa Creek, about fourteen miles south of the mouth of the Waikato River, which are described by the author in another paper in this volume (pp. 101-G). One — Chione auriculata n. sp. — was collected by the author when in company with Dr. Marshall at Pakaurangi Point, near Batley, Kaipara Harbour, in 1916 ; another- — Bittium oamaruticum n. sp. — was within a large gasteropod collected by Dr. Marshall from the Hutchinson's Quarry beds at Oamaru and given to the author; whilst there is one — Raeta (enuiplicata n. sp. — which was collected by Mr. E. P. Worley from the Okahukura Tunnel. All were submitted to the late Mr. H. Suter for identification, and pronounced by hnn to be new species. In addition to Chione auriculata n. sp. there was identified also by Mr. Suter, from the Pakaurangi Point beds, along with other fossils collected by the writer, a specimen of Mesalia striolata (Hutt.), a species not listed by Dr. Marshall in his recent paper.* Bittium oamaruticum n. sp. (Plate VII, fig. 1.) Very small elongate tapering shell of 11 very slightly convex whorls increasing gradually in size. Protoconch 2 J whorls, smooth : the other whorls with strong subvertical rounded axial ribs subequal in width to the interspaces, and made slightly nodular by 6 or 7 prominent rounded spiral threads with linear interspaces. The radial costae are 13 in number on later whorls, dying out on flattened base of body-whorl. Only one or two spiral threads on base below the angle of the body-whorl. Sinuous growth-lines distinct on base. Suture fairly deep, margined. Columella smooth, oblique, imperfect. Aperture imperfect, one-third of body-whorl being absent ; would appear to have been narrowly ovate and notched jiosteriorly. Inner lip very narrow, a mere film on body- whorl. Length, approximately 5 mm. ; diameter, 1-7 mm. . Holotype in Auckland University College collection. Localitv : Hutchinson's Quarrv beds. Collected by Dr. P. Marshall, 1917. Remarks. — Classed as a new species of the genus by the late Mr. H. Suter, though the lack of knowledge of the aperture appears to render the generic position somewhat uncertain. If correctly placed, this genus is now for the first time described fossil from New Zealand rocks. * P. Makshall, The Tertiary Molluscan Fauna of Pakaurangi Point, Kaipara Harbour, Trans. X.Z. hist., vol. 50, pp. 263-78, 1918. Bartrum. — New Fossil Mollusca. 97 Chione auriculata n. sp. (Plate VII, fig. 2.) Rounded-quadrate, small, rather compressed shell, almost equilateral ; posterior end squarely truncated. Lunule large, lanceolate, very sharply raised at dorsal margin into a prominent triangular ear-like portion ; margins sharply incised. Beaks rather small, little raised, approximate ; a distinct ridge from beak to lower angle of truncated posterior end of shell. Anterior dorsal margin forming triangular projection at lunule, the anterior side of triangle shortly forming an angle with the rounded anterior end. Posterior dorsal margin descends gently in convex curve to prominent angle with straightly truncated posterior end. Broadly rounded basal margin forms distinct angle at posterior end, and merges gradually into rounded anterior end. Concentric ornamentation prominent ; growth-lines are densely crowded and crossed by innumerable microscopic radiate lines. On lower half of shell are strong, broad, rounded lamellae, distant and somewhat irregular, 6 almost complete lamellae visible. They broaden out at posterior ridge of shell, and on dorsal portion beyond this are others nearer to the beak not developed anteriorly beyond this ridge. The lamellae crowd on the lunule, making it i:)laty. Hinge and other internal characters could not be observed. Length, 10-6 mm. ; height, 9 mm. ; diameter, 4-6 mm. Holotype in author's collection ; complete but for anterior half of left valve. Localitv : Pakaurangi Point, Kaipara Harbour. Collected by Bartrum, 1916. Circulus cingulatus ii. sp. (Plate VII, figs. 3 and 4.) Very small, umbilicate. almost discoidal shell, coiled in a very flat spiral. Whorls 3| or 4, very rapidly increasing, the protoconch smooth, the rest sculptured by prominent spiral, angular, sharply elevated raised bands : 5 of these are visible between the sutures on penultimate whorl, 15 on body- whorl, regularly distributed, about 8 on basal portion, but absent from umbilicus. Interspaces approximately ecjual in width to the ridges, striated strongly by closely spaced transverse growth-lines, which alone ornament umbilicus. Aperture somewhat incomplete, apparently circular, with a minute posterior sinus. Outer lip partially incomplete in holotype, moderately sharp, slightly crenate externally owing to spiral sculjjture. Inner lip fairly solid, forming partial margin to the umbilicus ; this latter not widely open and showing no coiling of whorls. Diameter, 4 mm. ; height, 1-9 mm. Holotype and two imperfect paratypes in author's collection. Localitv : Kawa Creek, south of Port Waikato. Collected by Bartrum, 1917. Remarks. — The late Mr. Suter remarked that this species comes nearest to C. politus Sut., from which, however, it is quite distinct. Raeta tenuiplicata n. sp. (Plate VII, figs. 5 and 6.) Shell of moderate size, very thin, obovate in outline, anterior end rounded, posterior produced and angled. Apparently agape anteriorly. Beaks directed forwards, sharp, fairly swollen, on posterior half of shell, approximate. From just below the beak a distinct wide shallow sinus passes 4 — Trans. 98 Transact ions. vertically to basal margin, giving shell a folded aspect. Anterior dorsal margin descends gradually, straight at first and then according with broadly convex anterior end. Posterior dorsal margin incomplete ; descends steeply, apparently slightly concave, to narrowly produced posterior end. Anterior end rather imperfect, but evidently angled with gently sinuous basal margin, which rises obliquely towards narrowing posterior end. Lunule not marked off, raised centrally, oval. Ornamentation shown only on isolated remnants of original surface ; narrow, shallow concentric grooves, somewhat irregularly excavated, closely spaced, about 2 per milli- metre. Radiate close lines visible on surface of cast but not on shell itself. Hinge and other internal characters unknown. Length, actual 37 mm., restored approximately 42 mm. ; height, 32 mm. ; diameter, 18 mm. Holotype and one paratype (both imperfect) in Auckland University College collection. Locality : Okahukura Tunnel. Collected by R. P. Worley, 1916. Siphonalia propenodosa n, sp. (Plate VII, figs. 7 and 8.) Oval turreted shell, solid, fairly large, closely approaching 8. nodosa (Mart.) but distinct in sculpture. Whorls 8J, protoconch apparently 2| whorls, the first smooth, the others axially costate. Spire short, angle 55°, whorls gradually increasing. Suture not impressed, slightly sinuous. Whorls somewhat angled, and lightly excavated above the angle. Aper- ture imperfect on the holotype, but well shown in a paratype ; high, oval ; outer lip fairly thin, slightly callous, and finely notched or crenulate within; faintly angled at both keels of body-whorl. Posterior notch very distinct ; anterior canal oblique, strongly recurved, broad, short, and truncated at base. Columella slightly excavated above and inflected to the left at canal. Inner lip spread broadly on body-whorl ; siphonal fascicle distinct, crossed by coarse lamellae. Height of aperture and canal about twice height of spire. Ornamentation of spiral threads especially strong on base of body-whorl and with finer interspaced threads particularly prominent there. On later spire-whorls and on body-whorl close below suture is a spiral row of minute elevated tubercles on a somewhat indistinct keel. On the whorls, at the prominent carina at the angle, is a conspicuous spiral band of about 11 sharp nodules merging in earlier spire-whorls into distinct costae which run to the anterior suture. Besides these two rows of tubercles on the body - whorl are two others — one prominent one on the lower of the carinae of the body- whorl, and a faint one on the base a little below this last. Growth-lines strongly shown and numerous on the body-whorl. Height, 32 mm. ; diameter, 18 mm. Holotype and two paratypes in author's collection. Locality : Coast near Kawa Creek, south of Waikato River, Auckland. Collected by Bartrum, 1917. Remarks. — The late Mr. Suter remarked : " Near S. nodosa (Mart.), but distinguished from it by the row of tubercles below the suture, and a fourth row upon the base. The former character brings it near S. conoidea (Zitt.), from which, however, it is quite distinct."'* * Personal communication. Bartrum. — New Fosxil MolJnsca. 99 Siphonalia kawaensis n. sp. (Plate VII, figs. 9 and 10.) Three specimens in a moderately good state of preservation ; that chosen as holotype is incomplete at the apex of the spire, but shows the aperture and ornamentation well. Shell oval, of medium size. Spire about half height of shell, angle 55°. Whorls about 8, gradually increasing. Protoconch (shown by a paratype), 2 J smooth whorls. In ornamentation identical with the preceding species, S. jnopenodosa, except that the spiral band of nodules on the base of the body-whorl is less distinct. Aperture oval, distinctly notched above, and passing below into a broad short greatly reflected oblique anterior canal, truncated at the base. Columella arcuate above, oblique below. Outer lip thin, sharply angled at upper carina of body-whorl, less so at lower one, somewhat crenulate within. Inner lip very broadly spread over body-whorl as a thick callosity, which is produced into a most conspicuous strong tooth- like process at about the middle height of aperture, just below the band of nodules on the base. Height, 43 mm. ; diameter, 25 mm. Holotype and two paratypes in author's collection. Locality : Coast near Kawa Creek, south of Waikato River, Auckland. Collected by Bartrum, 1917. Spisula aequilateralis gilberti n. var. (Plate VII, fi.g. 11.) A very plentiful pelecypod in the Kawa bed, but difficult to collect perfect on account of friability both of fossils and containing beds. Unfortunately the author's specimens were crushed in transit by post from the late Mr. Suter, who examined them, and are not therefore as desirable types as might be obtained. Shell moderately large, solid, with very heavy hinge with normal dentition and characters. In ornamentation the variety agrees with the normal species, the radial sculpture being perhaps closer and more distinct. In outline and contour there are constant differences. The variety is laterally more compressed, being less globose, and is flattened anteriorly on lower half of valve. The posterior dorsal margin descends rapidly from near the umbo and is straight, the dorsal region much flattened. The anterior dorsal area also is somewhat flatter than in the normal species. Length, 74 mm. ; height, 59 mm. ; half diameter, 17-5 mm. Holotype and imperfect paratype in author's collection. Locality : West coast, near Kawa Creek, south of Waikato River, Auckland. Collected by Bartrum, 1917. Terebra benesulcata n. sp. (Plate VII, fig. 12.) Small, cylindrico-conical shell, with sharp elongate spire. Whorls 7 in the incomplete holotype, rather flattish, gradually increasing ; suture rather deep. Spire about 4 times height of aperture. Protoconch absent. Growth-lines crowded, rather sinuous, specially distinct on penultimate and body whorls. Two spiral rows of strong rounded tubercles, the lower slightly the stronger, with a moderately deep broad sulcus between them, characterize the whorls. Ten tubercles on the penultimate whorl ; those of the lower row are continued as low costae to the anterior suture, but on the body-whorl die out before reaching the basal portion. No other spiral sculpture. 4* 1 00 Tra nsa c f ions . Aperture oval, lightly notched posteriorly, and produced anteriorly into a very short widely-open canal sharply bent to the left. Basal margin straight, not notched. Columella fairly short, straight, subvertical. Inner lip thinly and narrowly callous, ending in a point below. Outer lip incomplete. Siphonal fasciole distinct. Length of imperfect holotype. 9 mm. ; diameter, 2-3 mm. Holotype and two fragmentary paratypes in author's collection. Locality : West coast, near Kawa Creek, south of Waikato Eiver, Auck- land. Collected by Bartrum, 1917. Tugalia kawaensis n. sp. (Plate VII, fig. 13.) Small, conical, rounded shell, somewhat produced anteriorly ; sub- central, blunt apex, directed back. Posterior slope gentle, straight or only slightly concave, anterior gently convex. Posterior and lateral margins rounded, lateral margins converging towards broadly truncated anterior end. SUt-fasciole distinctly raised as sharp fold of shell, but not sculpturally differentiated except that it is stronger than adjacent radial riblets. These latter are well developed, about 50 in number, well raised, rounded. Some at intervals better developed than intervening ones ; interspaces subequal to ribs. Broad, concentric, rounded ribs, about 8 or 9 in number, are pro- minent in interspaces, and make the radial ribs themselves slightly nodular ; sjiecially prominent in the fragmentary paratype. Towards apex concentric and radial ribs alike diminish. The interior muscle-scar hooked back anteriorly towards apex. Length, 6-2 mm. ; breadth, 5-3 mm. ; height, 2-3 mm. Holotype and a fragmentary paratype in author's collection. Locality : West coast, near Kawa Creek, south of Waikato River, Auck- land. Collected by Bartrum, 1917. Turbo postulatus n. sp. (Plate VII, fig. 14.) Unfortunately only a fragment, comprising little more than the basal portion of the body-whorl, is available for description. It appeared to the writer to represent a species of Turbo previously unknown in the New Zealand fauna, a fact verified by the late Mr. Suter, who declared it to be a new species of that genus. In spite of the fragmentary nature of the holotype it seems advisable for convenience of reference to give this shell a specific name and to append its description. Shell fairly large, diameter approximately 27 mm., imperforate ; columella mainly straight, highly oblique, but bent to the right near produced basal margin of aperture. Outer lip imperfect, thin ; inner lip a widespread thin callosity on body-whorl and the somewhat excavated umbilical region, tapering rapidly to a point below. Sculpture of body-whorl distinctive : growth-lines very numerous and prominent, crossing several convex, broad, well-raised spiral keels, these latter separated by subequal interspaces. On the indefinitely delimited basal portion of the body-whorl are approximately 4 such keels. The fourth of these is much stronger and broader than the others ; it surrounds the relatively depressed umbilical tract and causes a distinct sinuosity of the basal margin of the aperture. Holotype in author's collection. Locality : West coast, near Kawa Creek, south of Waikato River, Auck- land. Collected by Bartrum, 1917. Trans. N.Z. Inst., Vol. LI. Plate VII. I-- A FlC4. I.— Fig. 2. — ( Figs . 3, 4. Fig. 5.— - Fig. 6.—. Fig. 7. — 1 Fig. 8.—. Fig. 9.— - Fig. 10—. Fig. 11.— Fig. 12.— F.G. IH.— Fig. 14.— '''(ice p . 100.] Bittiiitn oumurulicuni n. sp., 5 mm. x 1-7 mm. Chiotie auricidata n. sj)., 10-0 mm. x 9 mm. — Circulus cingulatus n. sp., holotype, diam. 4 mm. Ra'^tn tenHipliraUi. n. sp., holotyi)e, .37 mm. X 32 mm. Ra'"fa tenuiplkata n. sp., paratype. SipJ/onalia propenodosa n. sjj., jmratyps Siphonalirx propenodosa n. sp., holotype, 32 mm. x IS mm. Siphonalia Icaivaensis n. sp., holotype, 43mm. x 25mm. Siphoncdia kawuensis n. sp., paratyi)e. Spisula arquilaterali-s gilberti n. var., holotype, 74 mm. x 59 mm. Terebra benesulcata n. sj).. 9 mm. x 2 '3 mm. Tugalia Icaivaensis n. sp.. 6-2 mm. x 5-3 mm. Turbo posiulaliis n. sp., diam. approx. 27 mm. BartrUjVI. — A Fossiliferous Bed at Kama Creek. 101 Art. XIII.— .4 Fossiliferous Bed at Kawa Creek, West Coast, South of Waikato River, New Zealand. By J. A. Bartrum, Auckland University College. [Read before the Auckland Institute, 20th December, 19hS ; received by Editor 30th December, WIS ; issued seimrately, 26th May., lOJfJ.] Whilst on a liurried trip from Port Waikato to Raglan early in 1917 the writer observed at the coast near Kawa Creek, about fourteen miles south of the Waikato River, a very interesting section in the Tertiary succession and discovered a fossiliferous bed that had escaped the notice of earlier geologists examining the coast section. He was able later to spend about a day and a half collecting from this bed, in which he found molluscan fossils m great numbers, but very fragile and without great variety. No doubt, however, further collecting will add greatly to the present list of fauna. Even though incomplete, this list shows many points of interest and the object of this note is to illustrate these, and to publish some facts m connection with the more recent geological history of the Kawa Creek district that may have more than local interest, and help to throw light upon the mutual relationships of the later Notocene beds of a wide diastrophic district.* Resume of the Geology op Kawa Creek - Port Waikato District. The oldest rocks exposed m the area studied are Mesozoic shales, sand- stones, and local conglomerates, best exposed in the vicinity of Port Wai- kato They are disposed in a somewhat irregular asymmetrical anticline of which the axis is situated about half a mile east of the coast-line, to which its strike approximates. The western limb is the steeper, the dips there varying from 20° to 50°, whilst the strikes, unless where local complications occur, range approximately from north-west to N. 5° E. In the core of the anticline appear dark-grey to black marine shales with locally abundant belemnites, moderately frequent pelecypods and brachio- pods, and occasional gasteropods. Above these are well-bedded alternating sandstones and shales, with minor conglomerate, in which plant-remains are ubiquitous, and which furnish one of the best collecting-grounds for Mesozoic plants in New Zealand. The late Dr. E. A. Newell Arber has recently described the flora as Neocomian in age.f Resting discordantly upon the eroded edges of the Neocomian are lime- stones of the Notocene, usually fairly pure, but sometimes very marly Near their base they are strongly algal, and contain abundant fragments of the Mesozoic shales, a fact well shown near the mouth of the Huruwai Stream on the coast section. What fossils have been collected from these limestones have their analogues in the Oamaruian of other parts of New Zealand, t Warping, minor folding, and some faulting have caused the * J. A. Thomson, Diastrophic and other Considerations in Classification and Con-elation, and the Existence of Minor Diastrophic Districts in the Notocene, Trans. JS.Z. Inst., vol. 49, pp. 397-417, 1917. Ir^nJi^^ ^■.^''v'''^^ t''^''?.' ^^"^ ^^''^"' Mesozoic Floras of New Zealand, Palaeonto- logical Bvlletm Ao. 6, N.Z. Geological Survey, 1917. X Dr. -J. A. Thomson very kindly examined the brachiopods for the writer. 102 Transac/io/is. corresponding basal portions of these Oamaruian limestones to appear at very unequal heights above sea-level, whilst from many areas they have been removed by erosion, leaving the Mesozoic rocks exposed. The pre- Oamaruian surface of these last can only be surmised, for the evidence obtained is inconclusive, but it certainly appears to have possessed the broadness and simplicity so noticeable in the pre-Notocene surfaces of other parts of New Zealand.* Whatever may have been this surface, upon it was deposited the basal limestone, and then a sequence of marls, blue sandstones, and impure fine- grained limestones. Then came the gentle folding, or warping, with the accompanying minor faulting that has already been noted — movements that probably accompanied a period of relative land-elevation, evidenced near the Kawa Creek by the sharp planation of the edges of the upper beds of the Notocene sequence either by marine or subaerial erosion. The reverse swing of the oscillation now caused this surface of planation to be covered up by the fossiliferous marine sands that furnish one of the main objects of this article. Their fossils show that they are practically the uppermost Notocene, and it is probable that they are comparable with certain massive sandstones, discovered recently by Dr. Henderson in the Te Kuiti district, which unconformably overlie the upper beds of the Tertiary sequence in that area.t The closing members of the succession at the Kawa are not without interest, and may now be given. Unconformably above the fossiliferous sands is a local basaltic accumulation (both lava and agglomerate), followed by about 30 ft. of fresh-water silts, in which are intercalated a few thin, impure lignite-seams. Above these is a similar thickness of sands which appear to be wind-bedded ; then a bed of pumice silt — itself a most interest- ing discovery — which is followed by ancient dune sands rising to a height of nearly 400 ft. above sea-level, and more or less continuous north-west to Port Waikato. Details of the Coastal Section near Kawa Creek. Without entering upon a discussion of the relative merits of different lines of evidence in the correlation of the New Zealand Notocene beds, or of the vexed cjuestion of the substantial conformity or otherwise of these strata, the writer considers that in the instance he is describing the mutual stratigraphic relations of the beds have a very real importance. The physical unconformity is very marked, and if it is coeval with that described by Dr. Henderson in the Te Kuiti districtt it will no doubt serve a useful ])urpose in the classification of the latest Notocene strata of a wide district, if not of New Zealand. It seems desirable, therefore, to set forth in greater detail the observed section near the mouth of the Kawa Creek in which this unconformity is evident. It may be remarked, further, that there is a very definite disconforraity evident in the sea-cliffs immediately south of the Waikawau Stream, which is several miles north of the Kawa Creek, but this is in beds much below those at the latter locality. * See, for example, C. A. Cotton, The Structure and Later Geological History of New Zealand, Geol. May., dec. 6, vol. 3, pp. 2-48-19, 314-20, 1916. t J. Henderson, The Geology of the Te Kuiti Di.striet, with Special Reference to Coal Prospects, N.Z. Journ. Sci. <& Tech., vol. 1, p. 114, 1918. X J. Henderson, Joe. cit. Bartrum. — A Fossiliferoi/s Bed at Kauri Creel,-. 103 Amongst the lower beds of the observed section at the Kawa Creek locality are a series of thin greensand bands alternating with strong flaggy glauconitic limestone layers up to 1 ft. in thickness, the whole comprising a stratum about 15 ft. in depth, which strikes north and south and dips westward at approximately 15°. A normal strike fault traverses the section, accompanied by two lesser faults, and somewhat complicates its interpretation. This fault has a throw varying up to aijout 40 ft., and dips steeply eastward. Above the flaggy bands are bluish-white calcareous mudstones exposed for approximately 50 ft. of height in the sea-clifl"s ; they strike nearly north and south, and dip gently (at approximately 8°) westward. They are poorly fossiliferous, showing macroscopically merely a few sporadic Foraminifera and molluscs: Crepidula monoxijla (Less.) was the only specifically detei- minate mollusc collected. The greensand and flaggy calcareous bands just beneath contain very abundant Foraminifera and occasional distorted brachiopods. The former have been forwarded to Mr. F. Chapman, of Melbourne Museum, but his report upon them is not yet available. If one may judge from a rather limited number of fossils, mainly pelecy- pods, brachiopods, and echinoids, in beds of the same sequence but at a lower horizon, both sets of beds so far described — the flaggy bands and overlying mudstone — are probably Middle or U})per Oaniaruian in age.* The gently upturned edges of these beds are now most regularly trun- cated by an erosion-plane, rising from approximately 50 ft. above sea-level at the coastal section south of the Kawa Creek to about 80 ft. just north of the mouth of the Kawa, about half a mile distant. From its extreme regularity it would appear to be a result of marine planation, and it is clearly to be noted that this followed the gentle folding or warping and faulting which have just been described as apparent in the coast section. On the erosion surface rest yellow to bluish sands crowded with casts or actual shells of molluscs, a few bryozoans, corals, and other organisms. Near the base the remains are moderately well preserved, and have fur- nished the collection made by the author and listed in this paper. In depth these sands reach about 40 ft. They cannot be followed northward from the section now described, but what appears to be the same bed can be seen near where the coastal route regains the coast a mile or so south- wards after deviating inland to avoid some impassable basalt sea-cliffs, and again still farther south. f Here they have been disrupted by this basalt and overlain by columnar lava. At the more northerh^ locality, similarly, other lava or agglomerate rests on a locally irregular erosion surface of the fossiliferous sands, the agglomerate showing considerable variation in thickness, in places thinning to 1 ft. or so, in others thickening to as much as 20 ft. Close by is exposed part of the somewhat complex vent of the volcano, whence came this material, and whence poured forth a flood of basaltic lava reaching pro- bably several miles westward, for a small islet more than a mile from the shore appears to be basaltic. The columnar jointing of the flow renders it an easy prey to the great waves characteristic of this exposed coast. * -Ur. J. A. Thomson, who examined the bracliiopocls, reports that they are certainly Oamaruian. ■f" Hutton observed these beds and noted their unconformable relations to the underlying beds, but failed to obtain any marine fossils in them. He tentatively cor- related them with the Waitemata sandstones, but suspected that they might be much younger. (F. W. Hutton, On the Relative Ages of the Waitemata Series and the Brown Coal Series of Drury and Waikato, Trans. N.Z. Inst., vol. 3, jjp. 244-49, 1871.) 104 Transactions. Above the volcanic material come grey and white silts with impure lignite bands, all apparently of fluviatile origin, for they show good current- bedding in places. There is a depth of 30 ft. of these silts, which are then succeeded by an equal thickness of consolidated iron-stained sands, pro- bably of dune origin ; and again above these there is a most interesting bed, 10 ft. to 20 ft. in depth, of pumice silts, also evidently of fluviatile origin. A succession of dune-sands, rising to approximately 350 ft. above sea- level, and deeply stained and cemented by concretionary limonite, completes the section. All these beds above the fossiliferous sands are undoubtedly Noto- pleistocenef in age, and, though of considerable interest, are beyond the scope of this paper, which is chiefly concerned with the fossiliferous sands. J List of Mollusca from the Fossiliferous Sands. The Mollusca listed below come from near the base of the fossiliferous sands, and within a few feet, therefore, of the unconformity duly noted in the Kawa section. The identifications in nearly all cases were made or checked by the late Mr. H. Suter. For convenience of reference the genera are arranged in alphabetical order in the list. Recent species are preceded by an asterisk. Ancilla hehera (Hutt.). * novae-zelandiae (Sow.). *Anomia cf. huttoni Sut. *Arca novae-zelandiae Smith. — — subvelata Sut. *Barnea similis (Gray). *Calyptraea maculata (Q. & G.). *Cardiia calyculata (L.). *Chione mesodesyna (Q. & G.). meridional'is (Sow.). * spissa (Desh.). Cir cuius cingulatus Bartrum.§ Crepidula gregaria Sow. * monoxyla (Less.). striata (Hutt.). *Dentalium ? huttoni T. W. Kirk.|| jiareorense Pilsbry and Sharp. solidum Hutt. *Diplodo7ita zelandica (Gray). *Divaricella cumingi (Ad. & Ang.). *Dosinia anus (Phil.). * caerulea (Reeve). * magna Hutt. Drillia aequistriata Hutt. * laevis (Hutt.). *Emarginula striatula Q. & G. Fulgoraria sp. Glycymeris globosa (Hutt.). * striatularis (Lamk.). *Gomp]iina maorum Smith. ^ *Hipponix antiquatus (L.).** *Leda bellula A. Ad. Lima color ata Hutt. *Loripes concinna Hutt. *Mactra discors Gray. * scalpellum Reeve. Marginella ? harrisi Cossm. * pygmaea Sow. *Murex zelandicus Q. & G. *Myodora antipodum Smith. *Natica australis (Hutt.). * zelandica Q. & G. *Nucula hartvigiana Pfr. * nitidula A. Ad. Olivella neozelanica (Hutt.). Ostrea, several sp. t J. A. Thomson, loc. cit. X It is perhaps permissible to point out that the pumice silts oiTer strong evidence that the Waikato or some such river flowed westward to this portion of the coast in early Notopleistocene times, bringing the pumice from the central rhyolitic country. Pumice terraces of corresponding height above sea-level are described by Henderson on the banks of the Waikato River near Cambridge (J. Henderson, N.Z. Journ. Sci. <& Tech., vol. 1, pp. 112-15, 1918). § Described in this volume (p. 97). II Two specimens, small, incomplete at anterior end, come near D. huttoni, but ornamentation shows more numerous longitudinal ribs than in the type ^ Not before recorded fossil. ** New to fauna. Babteum. — A Fossiliferous B